Primary Device ID | 03700569639198 |
NIH Device Record Key | 86fdcd59-71fa-4a6e-adea-10661eb683ef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Newclip Instruments |
Version Model Number | ANC967 |
Catalog Number | ANC967 |
Company DUNS | 263281904 |
Company Name | NEWCLIP TECHNICS |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700569639198 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03700569639198]
Moist Heat or Steam Sterilization
[03700569639198]
Moist Heat or Steam Sterilization
[03700569639198]
Moist Heat or Steam Sterilization
[03700569639198]
Moist Heat or Steam Sterilization
[03700569639198]
Moist Heat or Steam Sterilization
[03700569639198]
Moist Heat or Steam Sterilization
[03700569639198]
Moist Heat or Steam Sterilization
[03700569639198]
Moist Heat or Steam Sterilization
[03700569639198]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-20 |
Device Publish Date | 2024-11-12 |