| Primary Device ID | 04046768000025 |
| NIH Device Record Key | e362dd1c-2c9d-44fe-8b93-9d5aaae41c4d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arm support |
| Version Model Number | 10016000 |
| Company DUNS | 315435859 |
| Company Name | MAQUET GmbH |
| 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 | 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 | 04046768000025 [Primary] |
| BWN | TABLE AND ATTACHMENTS, OPERATING-ROOM |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-30 |
| Device Publish Date | 2022-09-22 |
| 04046768130739 | 100232A0 |
| 04046768028524 | 100144F0 |
| 04046768028517 | 100144E0 |
| 04046768028494 | 100142A0 |
| 04046768001336 | 100144D0 |
| 04046768001329 | 100144C0 |
| 04046768000025 | 10016000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ARM SUPPORT 97229492 not registered Live/Pending |
Guo, Jinsheng 2022-01-20 |