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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
Open-surgery dissector FDA UDI
Device Name
V. Mueller Neuro/Spine SPINAL BODY DISSECTOR SMALL OVERALL LENGTH 8" (200MM) FDA UDI
Model / Reference
S-0051 FDA UDI
Description
V. Mueller Neuro/Spine SPINAL BODY DISSECTOR SMALL OVERALL LENGTH 8" (200MM) FDA UDI

Identifiers

Catalog Number
S-0051 FDA UDI
Primary DI / UDI-DI
10885403136870 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Open-surgery dissector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 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

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

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 6a55f7cf-2415-4fdb-bce5-9a583129a4a2 36 fields · synced Sep 18, 2026