Primary Device ID | 00815634020788 |
NIH Device Record Key | fe9c7847-bb47-40ef-93ba-6158c65e1405 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biomet Biologics |
Version Model Number | 800-0211 |
Company DUNS | 066839630 |
Company Name | Micromedics, 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 | true |
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 | 00815634020788 [Primary] |
CAN | Regulator, Pressure, Gas Cylinder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-13 |
Device Publish Date | 2023-12-05 |
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