Primary Device ID | 00848665002744 |
NIH Device Record Key | daee44c0-60c5-419f-86fd-3b784e816411 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FORCEPS LOBSTER CLAW, SERRATED |
Version Model Number | 0819 |
Company DUNS | 117858154 |
Company Name | ADVANCED ORTHOPEDIC SOLUTIONS 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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 00848665002744 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00848665002744]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-08-21 |
Device Publish Date | 2016-02-25 |
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