Primary Device ID | 08717127936144 |
NIH Device Record Key | cae6c2fa-8764-4069-ac84-41a50cf81aad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arion Magnide |
Version Model Number | Medium |
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 | 08717127936144 [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 |
08717127941278 | Application aid (donning and doffing) for medical compression garments |
08717127936472 | Application aid (donning and doffing) for medical compression garments |
08717127936151 | Application aid (donning and doffing) for medical compression garments |
08717127936144 | Application aid (donning and doffing) for medical compression garments. |