| Primary Device ID | 03700393300585 |
| NIH Device Record Key | 4015e71e-2c2b-4342-ac07-5f39a3317363 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | F5330 |
| Catalog Number | F5330 |
| Company DUNS | 265741780 |
| Company Name | PETERS SURGICAL |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +33470584170 |
| vectec@vectec.fr | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com | |
| Phone | +1 508-747-6033 |
| e.knupp@peters-surgical.com |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 330 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700393300127 [Primary] |
| GS1 | 03700393300585 [Package] Contains: 03700393300127 Package: Box [5 Units] In Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-09-20 |
| Device Publish Date | 2016-09-12 |
| 03661522100189 - OPTIME® | 2026-03-17 |
| 03661522100196 - OPTIME® | 2026-03-17 |
| 03661522100219 - OPTIME® | 2026-03-17 |
| 03661522100714 - OPTIME® | 2026-03-17 |
| 03661522100721 - OPTIME® | 2026-03-17 |
| 03661522100738 - OPTIME® | 2026-03-17 |
| 03661522100752 - OPTIME® | 2026-03-17 |
| 03661522100837 - CARDIOXYL® | 2026-03-17 |