Primary Device ID | 08717127936670 |
NIH Device Record Key | ba3751c6-d137-4617-945c-0b3d75ae8840 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arion Proth-Pro |
Version Model Number | Large |
Company DUNS | 489495862 |
Company Name | Arion Holding B.V. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 | true |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08717127936670 [Primary] |
IPM | Cover, Limb |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-13 |
Device Publish Date | 2023-11-03 |
08717127941285 | Donning aid for transfemoral prostheses |
08717127936670 | Donning aid for transfemoral prostheses |
08717127936663 | Donning aid for transfemoral prostheses |
08717127936656 | Donning aid for transfemoral prostheses |
08717127936571 | Donning aid for transfemoral prostheses |
08717127936564 | Donning aid for transfemoral prostheses |
08717127936526 | Donning aid for transfemoral prostheses |