Primary Device ID | J014660354820 |
NIH Device Record Key | 37edb9da-01ee-4da6-986c-ec79ea9d3438 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VENUS DIAMOND SYRINGE REFILL 1x4G C3 |
Version Model Number | 66035482 |
Catalog Number | 66035482 |
Company DUNS | 315666321 |
Company Name | Kulzer GmbH |
Device Count | 1 |
DM Exempt | true |
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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
J014647141980 - Signum liquid | 2024-11-29 Signum liquid, 4 ml |
J014660196750 - Signum matrix | 2024-11-29 Signum matrix (set) |
J014660196770 - Signum matrix | 2024-11-29 Signum matrix, OT1, 4 g |
J014660196780 - Signum matrix | 2024-11-29 Signum matrix, OT2, 4 g |
J014660196790 - Signum matrix | 2024-11-29 Signum matrix, OT5, 4 g |
J014660196800 - Signum matrix | 2024-11-29 Signum matrix, OT10, 4 g |
J014660196910 - Signum matrix | 2024-11-29 Signum matrix, MD1, 4 g |
J014660196920 - Signum matrix | 2024-11-29 Signum matrix, MD2, 4 g |