Primary Device ID | 08800019110668 |
NIH Device Record Key | 2754415e-3510-4d25-a72f-47f2bec5be4c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | POMO White |
Version Model Number | POMW |
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 | false |
Serial Number | true |
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 | 08800019110668 [Primary] |
KXR | Applicator, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-23 |
Device Publish Date | 2023-06-15 |
08800019110651 - POMO Black | 2023-06-23 |
08800019110668 - POMO White | 2023-06-23 |
08800019110668 - POMO White | 2023-06-23 |
08800019110675 - POMO Pink | 2023-06-23 |
08800019110712 - COMO Black | 2023-06-23 |
08800019110729 - COMO White | 2023-06-23 |
08800019110736 - COMO Pink | 2023-06-23 |
08800019110743 - COMO Tip | 2023-06-23 |
08800019110750 - COMO Tip | 2023-06-23 |