Identity
- Trade Name
- STINGRAY SURGICAL PRODUCTS FDA UDI
- Generic Name
- Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
- Device Name
- Reusable Bipolar Forceps Insulated, Malis, Bayonet, 8.5" (21.6cm), 0.5mm Tip, Non-Stick FDA UDI
- Model / Reference
- S03-675NS FDA UDI
- Description
- Reusable Bipolar Forceps Insulated, Malis, Bayonet, 8.5" (21.6cm), 0.5mm Tip, Non-Stick FDA UDI
Identifiers
- Catalog Number
- S03-675NS FDA UDI
- Primary DI / UDI-DI
- B112S03675NS0 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Stingray Surgical Products by Stingray Surgical Products L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Stingray Surgical Products L.l.c.
Sources (1)
- FDA UDI f9034720-e147-4d87-97b8-9f90db6d126e 36 fields · synced May 31, 2026