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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
Tympanotomy knife, reusable FDA UDI
Device Name
V. Mueller EAR BLADES 71NDK MYRINGOTOMY LANCE TIP FDA UDI
Model / Reference
AU05731-03 FDA UDI
Description
V. Mueller EAR BLADES 71NDK MYRINGOTOMY LANCE TIP FDA UDI

Identifiers

Catalog Number
AU0573103 FDA UDI
Primary DI / UDI-DI
10885403124440 FDA UDI
FDA Product Code
EMF FDA UDI
GMDN Term
Tympanotomy knife, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tympanotomy knife, reusable

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

Similar devices

Also classified as Tympanotomy knife, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 6f3e7e55-5a4e-4e12-be32-2f51877d5923 35 fields · synced Jun 8, 2026