Primary Device ID | 00810055471805 |
NIH Device Record Key | 6328f555-a1ee-4117-9493-d04a1ff83aea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Instrumentarium |
Version Model Number | L.71.210.H |
Company DUNS | 203088166 |
Company Name | Société Chirurgicale Instrumentarium Inc |
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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 00810055471805 [Primary] |
LRW | Scissors, General, Surgical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00810055471805]
Moist Heat or Steam Sterilization
[00810055471805]
Moist Heat or Steam Sterilization
[00810055471805]
Moist Heat or Steam Sterilization
[00810055471805]
Moist Heat or Steam Sterilization
[00810055471805]
Moist Heat or Steam Sterilization
[00810055471805]
Moist Heat or Steam Sterilization
[00810055471805]
Moist Heat or Steam Sterilization
[00810055471805]
Moist Heat or Steam Sterilization
[00810055471805]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-19 |
Device Publish Date | 2021-08-11 |