Identity
- Trade Name
- BLUEENDO FDA UDI
- Generic Name
- Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
- Device Name
- Tenaculum forceps Ø 13 / 10mm, WL 330mm, jaws Ø 10mm, double action, two teeth, ring handle stainless with flap-ratchet, non demountable, LL, stainless steel shaft, thread connection, incl. exchangeable outer tube FDA UDI
- Model / Reference
- 20-136510 FDA UDI
- Description
- Tenaculum forceps Ø 13 / 10mm, WL 330mm, jaws Ø 10mm, double action, two teeth, ring handle stainless with flap-ratchet, non demountable, LL, stainless steel shaft, thread connection, incl. exchangeable outer tube FDA UDI
Identifiers
- Catalog Number
- 501-990-203 FDA UDI
- Primary DI / UDI-DI
- 04251303811954 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- 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
Category: Rigid endoscopic tissue manipulation forceps, reusable
Blueendo by TROKAMED GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- TROKAMED GmbH
Sources (1)
- FDA UDI 89aafd40-1548-4d26-974e-2d9168b64225 35 fields · synced May 30, 2026