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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
General-purpose endoscopic needle, reusable FDA UDI
Device Name
V. Mueller Irrigation/Injection Needle, Cvd, Dia 1.2MM Overall Length 3-3/4-inch (9.5CM) FDA UDI
Model / Reference
CH3314 FDA UDI
Description
V. Mueller Irrigation/Injection Needle, Cvd, Dia 1.2MM Overall Length 3-3/4-inch (9.5CM) FDA UDI

Identifiers

Catalog Number
CH3314 FDA UDI
Primary DI / UDI-DI
10885403026652 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
General-purpose endoscopic needle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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: General-purpose endoscopic needle, reusable

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

Similar devices

Also classified as General-purpose endoscopic needle, 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 f44d31aa-49b6-4f18-9232-727a00567b2e 35 fields · synced Jun 8, 2026