Identity
- Trade Name
- ENDOPATH TRISTAR FDA UDI
- Generic Name
- Laparoscopic trocar blade, single-use FDA UDI
- Device Name
- Endopath Tristar Blunt Tip Surgical Trocars with Radiolucent Sleeves FDA UDI
- Model / Reference
- 512B FDA UDI
- Description
- Endopath Tristar Blunt Tip Surgical Trocars with Radiolucent Sleeves FDA UDI
Identifiers
- Catalog Number
- 512B FDA UDI
- Primary DI / UDI-DI
- 20705036012181 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Laparoscopic trocar blade, single-use 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Endopath Tristar by Ethicon Endo-Surgery, Inc. — 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
- Ethicon Endo-Surgery, Inc.
Sources (1)
- FDA UDI 79d3ad52-3fc2-4517-a061-f8f794891421 36 fields · synced Jun 1, 2026