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SilCut Scissor Punch

FDA UDI

Class I (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
SilCut Scissor Punch FDA UDI
Generic Name
Rigid endoscopic scissors, reusable FDA UDI
Device Name
SILCUT® PRO Scissors FDA UDI
Model / Reference
28571SP FDA UDI
Description
SILCUT® PRO Scissors FDA UDI

Identifiers

Catalog Number
28571SP FDA UDI
Primary DI / UDI-DI
04048551379028 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Rigid endoscopic scissors, 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

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: Rigid endoscopic scissors, reusable

SilCut Scissor Punch by Karl Storz GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 662f1407-0391-4b02-8bea-4834cbe11616 35 fields · synced May 30, 2026