Identity
- Trade Name
- Scissor Punch FDA UDI
- Generic Name
- Rigid endoscopic biopsy forceps, reusable FDA UDI
- Device Name
- Scissor Punch, 2.5 x 260mm FDA UDI
- Model / Reference
- 259-330-028 FDA UDI
- Description
- Scissor Punch, 2.5 x 260mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04049197514750 FDA UDI
- FDA Product Code
- HTX FDA UDI
- GMDN Term
- Rigid endoscopic biopsy forceps, 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
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
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: Rigid endoscopic biopsy forceps, reusable
Scissor Punch by RZ-Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscopic biopsy forceps, reusable.
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
- JACKSON BIOPSY FORCEPS — SONTEC INSTRUMENTS, INC. · Class I
- Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class II
- MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
- ELMED — ELMED INCORPORATED · Class II
- MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
- UTERINE BIOSPY TRIANGULAR BASKET PUNCH — SONTEC INSTRUMENTS, INC. · Class I
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
- RZ-Medizintechnik GmbH
Sources (1)
- FDA UDI 01e3aaed-7561-44ba-9f72-0699c580e87e 33 fields · synced May 30, 2026