Primary Device ID | 13760087126225 |
NIH Device Record Key | b0104eeb-6e0c-44b3-9678-1fb7d7322ed5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CRAWFORD HOOK |
Version Model Number | S1.1275 |
Company DUNS | 763408366 |
Company Name | FCI S A S FCI 20 22 |
Device Count | 1 |
DM Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 13760087126225 [Primary] |
HNQ | Hook, Ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[13760087126225]
Moist Heat or Steam Sterilization
[13760087126225]
Moist Heat or Steam Sterilization
[13760087126225]
Moist Heat or Steam Sterilization
[13760087126225]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-15 |
Device Publish Date | 2022-12-07 |
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