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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 SELVERSTONE INTERVERTEBRAL DISC RONGEUR FORCEPS STRAIGHT, JAWS 2 X 5MM SHAFT LENGTH 6 inches 15CM FDA UDI
Model / Reference
NL6081 FDA UDI
Description
V. Mueller SELVERSTONE INTERVERTEBRAL DISC RONGEUR FORCEPS STRAIGHT, JAWS 2 X 5MM SHAFT LENGTH 6 inches 15CM FDA UDI

Identifiers

Catalog Number
NL6081 FDA UDI
Primary DI / UDI-DI
10885403082061 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 f3a30645-bcbf-4e09-82a9-5fdf0698e932 35 fields · synced Jun 8, 2026