← Back to catalogue

V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Open-surgery dissector FDA UDI
Device Name
V. Mueller RHOTON BALL DISSECTOR TITANIUM, TIP 3MM WIDE OVERALL LENGTH 7-1/2 inches 19.1CM FDA UDI
Model / Reference
NL3785-16T FDA UDI
Description
V. Mueller RHOTON BALL DISSECTOR TITANIUM, TIP 3MM WIDE OVERALL LENGTH 7-1/2 inches 19.1CM FDA UDI

Identifiers

Catalog Number
NL378516T FDA UDI
Primary DI / UDI-DI
10885403201929 FDA UDI
FDA Product Code
GZX FDA UDI
GMDN Term
Open-surgery dissector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4525 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: Open-surgery dissector

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

Similar devices

Also classified as Open-surgery dissector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 9aa18c4f-e55a-4b1f-b9ad-29b6afb0b2d6 35 fields · synced Jun 8, 2026