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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
Suturing needle holder, reusable FDA UDI
Device Name
V. Mueller REPLACEMENT NEEDLE SMALL FOR YOUNG-MILLIN NEEDLE HOLDER (GU8580) FDA UDI
Model / Reference
GU8581-001 FDA UDI
Description
V. Mueller REPLACEMENT NEEDLE SMALL FOR YOUNG-MILLIN NEEDLE HOLDER (GU8580) FDA UDI

Identifiers

Catalog Number
GU8581-001 FDA UDI
Primary DI / UDI-DI
10885403050725 FDA UDI
FDA Product Code
FHR FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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 eb56ee42-f464-4dd5-b160-c550d306cb43 36 fields · synced Jun 6, 2026