| 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 |
| 03770034301158 - Synvisc | 2025-03-21 |
| 03770034301172 - Synvisc | 2025-03-21 |
| 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 |