Primary Device ID | 06970283131125 |
NIH Device Record Key | f11537c3-dfff-453b-abe7-e3e5ab5a46b8 |
Commercial Distribution Discontinuation | 2099-12-31 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Body Strap |
Version Model Number | 1001.59F0 |
Company DUNS | 545372336 |
Company Name | Maquet (Suzhou) Co. LTD |
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 | 06970283131125 [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 | 2022-12-15 |
Device Publish Date | 2022-12-07 |
06970283131125 | Accessories of Mobile Operating Table |
06970283131118 | Accessories of Mobile Operating Table |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BODY STRAP 74175815 1706385 Dead/Cancelled |
BOBBY W. BOYER 1991-06-11 |