Identity
- Trade Name
- YelloPort Plus FDA UDI
- Generic Name
- Electrocautery system handpiece FDA UDI
- Device Name
- LAPAROSCOPIC PORT ACCESS SYSTEM Optical handle Electrocautery System Handpiece FDA UDI
- Model / Reference
- YOH1201 FDA UDI
- Description
- LAPAROSCOPIC PORT ACCESS SYSTEM Optical handle Electrocautery System Handpiece FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05051986009339 FDA UDI
- 510(k) Number
- K070712 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Electrocautery system handpiece FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
No
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
YelloPort Plus by Surgical Innovations Limited — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Surgical Innovations Limited
Sources (1)
- FDA UDI 060e8a73-ec51-4b25-be9b-4bcaf5905a70 35 fields · synced Jun 1, 2026