Primary Device ID | 16949236203520 |
NIH Device Record Key | e265860b-acdf-4baa-afec-34e262d09bd4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | safety hypodermic needles |
Version Model Number | 21Gx1"(0.8x25mm) |
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 | 06949236203523 [Primary] |
GS1 | 16949236203520 [Package] Contains: 06949236203523 Package: [100 Units] In Commercial Distribution |
GS1 | 26949236203527 [Package] Package: [20 Units] In Commercial Distribution |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-29 |
Device Publish Date | 2022-11-21 |
06949236204070 | 23G×38mmTW |
06949236204049 | 23G×25mmTW |
06949236204018 | 25G×25mmRW |
16949236203605 | 30Gx1/2"(0.31x13mm) |
16949236203599 | 27Gx1/2"(0.4x13mm) |
16949236203582 | 25Gx1"(0.5x25mm) |
16949236203575 | 25Gx5/8"(0.5x16mm) |
16949236203568 | 23Gx1"(0.6x25mm) |
16949236203551 | 22Gx1 1/2"(0.7x38mm) |
16949236203544 | 22Gx1"(0.7x25mm) |
16949236203537 | 21Gx1 1/2"(0.8x38mm) |
16949236203520 | 21Gx1"(0.8x25mm) |
16949236203513 | 20Gx1"(0.9x25mm) |
16949236203506 | 18Gx1 1/2"(1.2x38mm) |
16949236203490 | 18Gx1"(1.2x25mm) |