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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
Rigid endoscopic grasping forceps, reusable FDA UDI
Device Name
ENDOLAP 10MM STAINLESS STEEL SPOON GRASPER W/FLUSHABLE PORT, 32CM FDA UDI
Model / Reference
F260.05 FDA UDI
Description
ENDOLAP 10MM STAINLESS STEEL SPOON GRASPER W/FLUSHABLE PORT, 32CM FDA UDI

Identifiers

Catalog Number
F260.05 FDA UDI
Primary DI / UDI-DI
10885403040313 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid endoscopic grasping forceps, 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 b867273c-6784-4926-91ca-7d4b91fd66c7 36 fields · synced Jun 8, 2026