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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
Dressing/utility forceps, tweezers-like, reusable FDA UDI
Device Name
DE BAKEY Forceps Atraumatic Str 1.5mm 20cm/8" FDA UDI
Model / Reference
16-306-20 FDA UDI
Description
DE BAKEY Forceps Atraumatic Str 1.5mm 20cm/8" FDA UDI

Identifiers

Catalog Number
16-306-20 FDA UDI
Primary DI / UDI-DI
08403207000293 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Dressing/utility forceps, tweezers-like, 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 — 8 Inch FDA UDI

Category: Dressing/utility forceps, tweezers-like, 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 Dressing/utility forceps, tweezers-like, 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 63d6d184-ca06-4213-9014-a192e56c9217 36 fields · synced Jun 1, 2026