Primary Device ID | G2021401694140 |
NIH Device Record Key | 1d6c257f-84db-4693-be2d-6e7902d2dd7a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgical Scissor |
Version Model Number | 140169414 |
Catalog Number | 14-01694-14 |
Company DUNS | 645816062 |
Company Name | CONCISE ENTERPRISES |
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 | true |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | G2021401694140 [Primary] |
LRW | Scissors, General, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-12 |
Device Publish Date | 2023-12-04 |
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