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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
Intrauterine cannula, reusable FDA UDI
Device Name
FLEXIBLE EXTENSION TIP ONLY FOR KAHN CANNULA FDA UDI
Model / Reference
GL2360-002 FDA UDI
Description
FLEXIBLE EXTENSION TIP ONLY FOR KAHN CANNULA FDA UDI

Identifiers

Catalog Number
GL2360002 FDA UDI
Primary DI / UDI-DI
70885403159956 FDA UDI
FDA Product Code
HES FDA UDI
GMDN Term
Intrauterine cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1300 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: Intrauterine cannula, reusable

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

Similar devices

Also classified as Intrauterine cannula, 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 4f9e34e7-704d-4ba6-bc57-63e80e11a4f1 35 fields · synced Jun 8, 2026