Primary Device ID | 00840117340930 |
NIH Device Record Key | 3aced053-67d1-4d76-990c-ac5cb41c56ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biopsy Punches, Sterile, Mixed Box |
Version Model Number | 4097 |
Company DUNS | 008124539 |
Company Name | Dynarex Corporation |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840117340930 [Primary] |
GS1 | 00840117340954 [Package] Package: Box [25 Units] In Commercial Distribution |
GS1 | 00840117340978 [Package] Contains: 00840117340954 Package: Shipper [24 Units] In Commercial Distribution |
LRY | Punch, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2025-04-08 |
Device Publish Date | 2022-05-23 |
00840117323674 | Biopsy Punches, Sterile, Mixed Box, 5 each of 2.0 mm, 3.0 mm, 4.0 mm, 5.0 mm, 6.0 mm |
00840117340930 | Biopsy Punches, Sterile, Mixed Box, 5 each of 2.0 mm, 3.0 mm, 4.0 mm, 5.0 mm, 6.0 mm |