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V. Mueller

FDA UDI

Class II (US FDA UDI)

by Carefusion 2200, Inc

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
V. Mueller 5MM INTRODUCER SLEEVE FOR ENDO-LOOP, 17CM FDA UDI
Model / Reference
F283.00 FDA UDI
Description
V. Mueller 5MM INTRODUCER SLEEVE FOR ENDO-LOOP, 17CM FDA UDI

Identifiers

Catalog Number
F283.00 FDA UDI
Primary DI / UDI-DI
10885403040535 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not 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

V. Mueller by Carefusion 2200, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 13eb68fd-8adc-4f62-a762-e5b54123f5cd 36 fields · synced Jun 8, 2026