LUFS200D1Liquid VFFS Sachet Filling Machine
Compact piston-pump VFFS platform for sauces, syrups, gels and other flowable products.
Flexible single-lane auger VFFS platform for powder packs from small sachets to larger bags.

Machine overview
The LU-FS06 is a single-lane auger-fed VFFS machine with a broad reference bag envelope. It can be configured for powdered food, nutritional, cosmetic and compatible industrial products where roll-stock packaging is appropriate.
Published specification
| Electrical supply | 110 V or 220 V, 50–60 Hz |
|---|---|
| Indicative speed | Approximately 5–80 bags per minute |
| Reference volume range | Approximately 150–2000 ml |
| Maximum film width | Approximately 520 mm |
| Reference bag width | 60–250 mm |
| Reference bag length | 80–350 mm |
| Compressed air | Approximately 0.6–0.8 MPa |
| Approximate weight | 500 kg |
Reference figures are configuration-dependent and must be confirmed for the product, pack and utilities.
Configure the line
Performance validation
Target output and dose repeatability are affected by product flow, environmental conditions, sachet length, film sealing window, changeover and quality-control settings. Supply representative product and production film for a meaningful test.
Related machinery
LUFS200D1Compact piston-pump VFFS platform for sauces, syrups, gels and other flowable products.
LU-FSMP8High-output multi-lane VFFS system with independent magnetic-pump dosing for narrow liquid sachets.
LU-FSFM6Independent auger dosing across multiple lanes for high-output powder sachet production.
Common questions
Output varies with dose size, bag length, powder settling, auger revolutions, sealing time and downstream inspection. A trial provides the most useful production estimate.
The reference specification is volumetric. Powder mass depends on bulk density, so the machine should be selected against actual target weights and product samples.
Yes, within the machine envelope and with suitable forming sets, auger tooling and recipes. Changeover time should be considered during line design.
Tell us about your product and pack
Send the product, target dose, sachet dimensions, film and required output. Lancing Ltd will review your application and recommend a practical machinery route before a detailed quotation.
Production specification for LU-FS06
The published volume, film-width and speed references cover a broad configuration range. A specific powder, dose and bag format will occupy only part of that envelope, and auger tooling, forming parts and product feed must be selected for the actual project.
A screw selected for a larger dose may not provide the required control at the lowest dose, while a small auger can restrict output at the upper end. The full dose matrix should be reviewed before deciding how many auger, tube and funnel sets are required.
Film width, bag width and length also affect the forming set, product drop and sealing cycle. Performance should be demonstrated on the commercially important combinations rather than assuming that one successful midpoint format proves the entire range.
| Dose extremes | Trial the lowest and highest commercial doses using the relevant auger and normal product condition. |
|---|---|
| Format extremes | Run the smallest and largest critical bag or sachet, including registered print, coding and tear features where required. |
| Powder feed | Reproduce the intended hopper refill or transfer system and observe dose stability before and after replenishment. |
| Cleaning and setup | Demonstrate access, removal and refitting of product-contact and change parts and verify the next approved recipe. |
| Output record | Measure accepted packs for each critical product-format combination and state all stops, rejects and inspection intervals. |
A modest output and limited floor space may favour the compact LUFM1000 route, while sustained production of narrow identical sachets can justify a multi-lane system. The correct comparison uses the same product and accepted-pack definition.
A useful trial record identifies the product and film batches, dose setting, sachet dimensions, forming and sealing parts, coding setup, operating speed, stops, rejected packs and quality checks. Retained samples should be labelled so results can be traced to the lane, recipe or test condition where relevant.
The final quotation and acceptance schedule should distinguish indicative catalogue references from the values that will be demonstrated with the agreed product, pack and utilities.
Additional buyer questions
No. It is an indicative reference across configurations. Actual output depends on powder, dose, bag length, film, coding, sealing, feeding and quality-control conditions.
The dosing principle and product path may need substantial changes. Free-flowing or fragile granules can be better suited to weighing or another dosing system.
Auger resolution, cutoff and product aeration can make the lowest dose the most demanding. A midpoint result does not prove the lower end of a wide range.
State available pressure, flow, quality and connection point under operating conditions. The final requirement must be confirmed for the supplied configuration.
Define the project around your product and pack
Provide representative product, every required dose and sachet size, film details, accepted output, utilities, cleaning and inspection requirements. Lancing Ltd can then confirm whether the LU-FS06 is the correct starting point and define the trial scope.
Model-specific evidence schedule
A broad reference range can require different auger, forming and sealing configurations. Treat every commercial product/pack combination as part of the machine specification.
| Powder state | Record batch, bulk density, aeration, moisture, dust and feed method at start-up, steady run, refill, low level and restart. |
|---|---|
| Auger configuration | Identify screw, tube, agitation, hopper level controls and recipe used for every trialled dose family. |
| Format configuration | Identify forming parts, film web, jaws, cut/notch, registration and coder for each critical pack family. |
| Accepted evidence | Time-identified dose results, clean seals, integrity checks, retained packs, rejected examples, changeover record and accepted output. |