Primary Device ID | 10603354130163 |
NIH Device Record Key | c82c9991-9b29-4d6d-b65e-4a2a69f85ce1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BAM |
Version Model Number | REV00 |
Catalog Number | A0163A1 |
Company DUNS | 150600252 |
Company Name | EHOB INC |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10603354130163 [Primary] |
GS1 | 30603354130105 [Package] Package: [20 Units] In Commercial Distribution |
FMR | Device, Transfer, Patient, Manual |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-09 |
Device Publish Date | 2024-05-01 |
30603354130129 | BAM Pro XL System – 1 ea |
10603354130170 | BAM Pro XL Repositioning Sheet with ComfortTop ES XL – 1 ea |
10603354130163 | BAM Pro XL Repositioning Sheet – 1 ea |
30603354130099 | BAM Pro System – 1 ea |
10603354130149 | BAM Pro Repositioning Sheet with ComfortTop ES – 1 ea |
10603354130132 | BAM Pro Repositioning Sheet – 1 ea |