Identity
- Trade Name
- Tontarra Medizintechnik GmbH FDA UDI
- Generic Name
- Bone punch, reusable FDA UDI
- Device Name
- PITUITARY Rongeur 30° angled up; 6mm; coated 232mm FDA UDI
- Model / Reference
- 240-604-06KGCC FDA UDI
- Description
- PITUITARY Rongeur 30° angled up; 6mm; coated 232mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04050183353536 FDA UDI
- FDA Product Code
- HTX FDA UDI
- GMDN Term
- Bone punch, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone punch, reusable
Tontarra Medizintechnik GmbH by Tontarra Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone punch, reusable.
- Kwik Kleen — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II
- Quick Release — Vitalitec International Medizintechnik GmbH · Class II
- Quick Release — Vitalitec International Medizintechnik GmbH · Class II
- Legion — Smith & Nephew, Inc. · Class II
- Quick Release — Vitalitec International Medizintechnik GmbH · Class II
- Quick Release — Vitalitec International Medizintechnik GmbH · Class II
- Kwik Kleen — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II
- Punch — SOPRO-COMEG GmbH · Class II
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tontarra Medizintechnik GmbH
Sources (1)
- FDA UDI b2bd46a4-73e5-48b9-9b0b-5053f76c3264 34 fields · synced May 30, 2026