Primary Device ID | 10810113575398 |
NIH Device Record Key | d90f02b9-570a-417b-b024-e9ba48a34d77 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cyrogrid |
Version Model Number | SUP3050 |
Company DUNS | 047025993 |
Company Name | VIVE HEALTH LLC |
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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810113575391 [Primary] |
GS1 | 10810113575398 [Package] Contains: 00810113575391 Package: Case [6 Units] In Commercial Distribution |
ITQ | Joint, Knee, External Brace |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-19 |
Device Publish Date | 2024-01-11 |
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