Primary Device ID | 04260647941517 |
NIH Device Record Key | dc8d2dc3-7c4a-45ca-b6b3-148991955027 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AKRUS |
Version Model Number | AK 5010MBS |
Company DUNS | 324099522 |
Company Name | AKRUS GmbH & Co. KG |
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 | true |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04260647941517 [Primary] |
GBB | Chair, Surgical, Ac-Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-12 |
Device Publish Date | 2023-12-04 |
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