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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
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Device Name
V. Mueller VATS SEMB CLAMP 140MM FUL CVD 1X2, 10MM withRAT WORKING LENGTH 12.25 inches 31CM OVERALL LENGTH 15.5 inches 39.5CM FDA UDI
Model / Reference
CH1811 FDA UDI
Description
V. Mueller VATS SEMB CLAMP 140MM FUL CVD 1X2, 10MM withRAT WORKING LENGTH 12.25 inches 31CM OVERALL LENGTH 15.5 inches 39.5CM FDA UDI

Identifiers

Catalog Number
CH1811 FDA UDI
Primary DI / UDI-DI
10885403180880 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

No

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: Surgical soft-tissue manipulation forceps, scissors-like, reusable

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, scissors-like, 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 e8162061-d030-4d93-8bf4-91df5d7b61a2 35 fields · synced Jun 8, 2026