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Scissor Punch

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
Scissor Punch FDA UDI
Generic Name
Bone-coring punch, reusable FDA UDI
Device Name
Scissor Punch, Up Angle 3.5 x 260mm FDA UDI
Model / Reference
259-330-534 FDA UDI
Description
Scissor Punch, Up Angle 3.5 x 260mm FDA UDI

Identifiers

Primary DI / UDI-DI
04049197518024 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Bone-coring 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone-coring punch, reusable

Scissor Punch by RZ-Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-coring punch, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cb5b9055-eb00-481e-bb0e-6f5640c39616 33 fields · synced May 30, 2026