Primary Device ID | 07640243231217 |
NIH Device Record Key | 7da1d444-a318-43a0-b16a-0900ba4fc40f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Imetric |
Version Model Number | RSB-48-23-06-14-08 |
Catalog Number | RSB-48-23-06-14-08 |
Company DUNS | 482203390 |
Company Name | Imetric 4D Imaging Sàrl |
Device Count | 8 |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640243231200 [Primary] |
GS1 | 07640243231217 [Unit of Use] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07640243231217]
Moist Heat or Steam Sterilization
[07640243231217]
Moist Heat or Steam Sterilization
[07640243231217]
Moist Heat or Steam Sterilization
[07640243231217]
Moist Heat or Steam Sterilization
[07640243231217]
Moist Heat or Steam Sterilization
[07640243231217]
Moist Heat or Steam Sterilization
[07640243231217]
Moist Heat or Steam Sterilization
[07640243231217]
Moist Heat or Steam Sterilization
[07640243231217]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-14 |
Device Publish Date | 2025-08-06 |