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V. Mueller

FDA UDI

Class I (US FDA UDI)

by Carefusion 2200, Inc

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Neurosurgical sponge FDA UDI
Device Name
V. Mueller STERILE PATTIES COTTON 1/2X1/2IN 200/BX FDA UDI
Model / Reference
NL9051 FDA UDI
Description
V. Mueller STERILE PATTIES COTTON 1/2X1/2IN 200/BX FDA UDI

Identifiers

Catalog Number
NL9051 FDA UDI
Primary DI / UDI-DI
10885403128479 FDA UDI
FDA Product Code
GDY FDA UDI
GMDN Term
Neurosurgical sponge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4450 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

V. Mueller by Carefusion 2200, Inc — Class I — 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 3579a8af-cf53-4e2d-b596-679dd15b6369 36 fields · synced Jun 8, 2026