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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
Scalpel handle, reusable FDA UDI
Device Name
V. Mueller NO 7 KNIFE HANDLE FOR BLADES 10, 11, 12 and 15 OVERALL LENGTH 6-3/8 inches 16.2CM FDA UDI
Model / Reference
SU1407 FDA UDI
Description
V. Mueller NO 7 KNIFE HANDLE FOR BLADES 10, 11, 12 and 15 OVERALL LENGTH 6-3/8 inches 16.2CM FDA UDI

Identifiers

Catalog Number
SU1407 FDA UDI
Primary DI / UDI-DI
10885403059599 FDA UDI
FDA Product Code
GDZ FDA UDI
GMDN Term
Scalpel handle, 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

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: Scalpel handle, reusable

A comprehensive overview of the V. Mueller NO 7 KNIFE HANDLE FOR BLADES 10, 11, 12 and 15 OVERALL LENGTH 6-3/8 inches 16.2CM medical device, including its features, compliance information, and FAQs.

Similar devices

Also classified as Scalpel handle, 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 d00265d5-0e54-4cb0-bbc0-f1db86dc6434 35 fields · synced Jul 18, 2026