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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-purpose surgical scissors, reusable FDA UDI
Device Name
MAYO Scss Str 23cm/9" FDA UDI
Model / Reference
11-160-23 FDA UDI
Description
MAYO Scss Str 23cm/9" FDA UDI

Identifiers

Catalog Number
11-160-23 FDA UDI
Primary DI / UDI-DI
08403207160232 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
General-purpose surgical scissors, 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 — 9 Inch FDA UDI

Category: General-purpose surgical scissors, 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-purpose surgical scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4d72df9b-957d-482c-8191-41cd09f5e896 36 fields · synced Jun 8, 2026