Primary Device ID | 10603354130057 |
NIH Device Record Key | 2a5c7a60-7df0-4da6-9607-d7a071722991 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BAM Sheet |
Version Model Number | REV00 |
Catalog Number | A0159A1 |
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 | 10603354130057 [Primary] |
GS1 | 30603354130068 [Package] Package: Box [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 | 2023-05-16 |
Device Publish Date | 2023-05-08 |
30603354130044 | XL BAM Sheet - Single |
30603354130020 | Standard BAM Sheet - Single |
10603354130057 | Short BAM Sheet - Single |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BAM SHEET 97612441 not registered Live/Pending |
EHOB, Inc. 2022-09-29 |