Primary Device ID | 06949236200539 |
NIH Device Record Key | dbefa89c-31a4-488c-b067-5193c28b5e9f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Insulin Pen Needle |
Version Model Number | 0.33×12mm |
Company DUNS | 529239746 |
Company Name | Berpu Medical Technology Co.,Ltd |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06949236200171 [Primary] |
GS1 | 06949236200355 [Package] Contains: 06949236200171 Package: [100 Units] In Commercial Distribution |
GS1 | 06949236200539 [Package] Contains: 06949236200355 Package: [50 Units] In Commercial Distribution |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-20 |
Device Publish Date | 2016-09-15 |
06949236200539 | 0.33×12mm |
06949236200522 | 0.33×8mm |
06949236200515 | 0.33×6mm |
06949236200508 | 0.33×5mm |
06949236200492 | 0.30×12mm |
06949236200485 | 0.30×10mm |
06949236200478 | 0.30×8mm |
06949236200461 | 0.30*6mm |
06949236200454 | 0.30×5mm |
06949236200447 | 0.25×12mm |
06949236200430 | 0.25×8mm |
06949236200423 | 0.25×6mm |
06949236200416 | 0.25×5mm |
06949236200409 | 0.25×4mm |
06949236200393 | 0.23×8mm |
06949236200386 | 0.23×6mm |
06949236200379 | 0.23×5mm |
06949236200362 | 0.23×4mm |