Primary Device ID | 03770034301134 |
NIH Device Record Key | 4f4db8c7-526f-458f-ac08-007b533c8792 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD |
Version Model Number | Insyte Autoguard Winged |
Company DUNS | 281488639 |
Company Name | UNIVERDERM |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |
---|---|
GS1 | 03770034301134 [Package] Contains: 03770034301141 Package: [50 Units] In Commercial Distribution |
GS1 | 03770034301141 [Primary] |
FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-07 |
Device Publish Date | 2025-01-30 |
03770034301134 - BD | 2025-02-07 |
03770034301134 - BD | 2025-02-07 |
03770034301097 - Radiesse | 2024-12-10 |
03770034301127 - Sculptra | 2024-12-10 |
03770034301110 - Restylane Eyelight | 2024-12-03 |
03770034301004 - Juvederm | 2024-03-05 |
03770034301011 - Juvederm | 2024-03-05 |
03770034301028 - Restylane | 2024-03-05 |
03770034301035 - Restylane | 2024-03-05 |