Primary Device ID | 07640243230142 |
NIH Device Record Key | 4ca5ccb7-5d31-4035-afbc-b2a7146ef37e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Imetric |
Version Model Number | ICB-48-23S-09-16 |
Catalog Number | ICB-48-23S-09-16 |
Company DUNS | 482203390 |
Company Name | Imetric 4D Imaging Sàrl |
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 | true |
Serial Number | false |
Manufacturing Date | true |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640243230142 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07640243230142]
Moist Heat or Steam Sterilization
[07640243230142]
Moist Heat or Steam Sterilization
[07640243230142]
Moist Heat or Steam Sterilization
[07640243230142]
Moist Heat or Steam Sterilization
[07640243230142]
Moist Heat or Steam Sterilization
[07640243230142]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-23 |
Device Publish Date | 2024-12-13 |