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), 0.7mm Tip, Stainless Steel, Up 30 FDA UDI
- Model / Reference
- S03-676U30 FDA UDI
- Description
- Reusable Bipolar Forceps Insulated, Malis, Bayonet, 8.5" (21.6cm), 0.7mm Tip, Stainless Steel, Up 30 FDA UDI
Identifiers
- Catalog Number
- S03-676U30 FDA UDI
- Primary DI / UDI-DI
- B112S03676U300 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
A comprehensive overview of the STINGRAY SURGICAL PRODUCTS device, including its features, compliance, and regulatory status.
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 cc229907-cf3f-44f1-9488-285b7f95fff7 36 fields · synced Jun 26, 2026