| Primary Device ID | 30603354130020 |
| NIH Device Record Key | b0015b41-d1f8-4d2f-adda-3b9fbcd9072e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BAM Sheet |
| Version Model Number | REV00 |
| Catalog Number | A0154A1 |
| 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 | 10603354130019 [Primary] |
| GS1 | 30603354130020 [Package] Contains: 10603354130019 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 | 2023-02-09 |
| Device Publish Date | 2023-02-01 |
| 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 |