Primary Device ID | 06949236205046 |
NIH Device Record Key | 875fbb4b-afad-4bde-93a5-c13fdb26d123 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | hypodermic syringes |
Version Model Number | 1ml 25G×25mmRW |
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 | 06949236205039 [Primary] |
GS1 | 06949236205046 [Package] Contains: 06949236205039 Package: [100 Units] In Commercial Distribution |
GS1 | 06949236205053 [Package] Package: [12 Units] In Commercial Distribution |
GS1 | 06949236205121 [Package] Package: [10 Units] In Commercial Distribution |
FMF | Syringe, Piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2020-09-01 |
06949236205046 | 1ml 25G×25mmRW |
06949236205015 | 1ml 23G×25mmTW |
06949236205213 | 3ml 25G×25mm RW |