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V. Mueller

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
V. Mueller Neuro/Spine T-COAT MICRO-HANDLE KERRISON RONGEUR 40DEG UPCUTTING 3MM BITE, 15MM OPENING SHAFT LENGTH 12 inches 30.5CM FDA UDI
Model / Reference
NL4255-23T FDA UDI
Description
V. Mueller Neuro/Spine T-COAT MICRO-HANDLE KERRISON RONGEUR 40DEG UPCUTTING 3MM BITE, 15MM OPENING SHAFT LENGTH 12 inches 30.5CM FDA UDI

Identifiers

Catalog Number
NL425523T FDA UDI
Primary DI / UDI-DI
10885403077098 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Spinal rongeur FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 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: Spinal rongeur

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

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI bfb27c4b-fa08-4422-8b69-d6f96dc9c1b7 35 fields · synced Jun 8, 2026