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V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Neurosurgical scissors FDA UDI
Device Name
V. Mueller YASARGIL MICRO SCISSORS BAYONET SHAPE, STRAIGHT BLADE LENGTH 12.5MM OVERALL LENGTH 8 inches 20.3CM FDA UDI
Model / Reference
NL4003 FDA UDI
Description
V. Mueller YASARGIL MICRO SCISSORS BAYONET SHAPE, STRAIGHT BLADE LENGTH 12.5MM OVERALL LENGTH 8 inches 20.3CM FDA UDI

Identifiers

Catalog Number
NL4003 FDA UDI
Primary DI / UDI-DI
10885403075346 FDA UDI
FDA Product Code
GZX FDA UDI
GMDN Term
Neurosurgical scissors FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4525 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: Neurosurgical scissors

V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 0430dcae-a8ce-43bb-bab1-76a04488616c 35 fields · synced Jun 8, 2026