| Primary Device ID | M209181000 |
| NIH Device Record Key | 5ac6edba-634a-4395-b20e-a9068916bd36 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Towel Clamp |
| Version Model Number | 18100 |
| Company DUNS | 618749857 |
| Company Name | BIOPRO, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M209181000 [Primary] |
| HXD | Clamp |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
[M209181000]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-05-03 |
| Device Publish Date | 2019-05-09 |
| 00810012485685 | 18100 |
| M209181000 | 18100 |