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Anmuth Medical International

FDA UDI

Class I (US FDA UDI)

by Anmuth Medical International Llc

Identity

Trade Name
Anmuth Medical International FDA UDI
Generic Name
General surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
LARGE SPOON 7.5" OVERALL LENGTH FDA UDI
Model / Reference
90-129-19 FDA UDI
Description
LARGE SPOON 7.5" OVERALL LENGTH FDA UDI

Identifiers

Catalog Number
90-129-19 FDA UDI
Primary DI / UDI-DI
08403207009692 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
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

No

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

Dimensions & Sizes

Size
Length — 7.5 Inch FDA UDI

Category: General surgical procedure kit, non-medicated, reusable

Anmuth Medical International by Anmuth Medical International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Anmuth Medical International Llc

Sources (1)

  • FDA UDI ee84fac0-dd03-4030-9a0c-91531c8ad4a8 36 fields · synced May 30, 2026