Primary Device ID | 08800019151012 |
NIH Device Record Key | 29a34271-d7e2-4dbc-a9bc-25f7806f6f5d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BL Clamp |
Version Model Number | CLAMP1 |
Company DUNS | 687338285 |
Company Name | B& L Biotech, 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 | false |
Lot Batch | true |
Serial Number | false |
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 | 08800019151012 [Primary] |
EJG | Forceps, Rubber Dam Clamp |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
[08800019151012]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-28 |
Device Publish Date | 2025-07-18 |
08800019151067 | CLAMP211 |
08800019151050 | CLAMP210 |
08800019151043 | CLAMP201 |
08800019151036 | CLAMP13A |
08800019151029 | CLAPM12A |
08800019151012 | CLAMP1 |