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: Neurosurgical probe FDA UDI
Device Name: Probe Double End 15cm FDA UDI
Model / Reference: 26-106-16 FDA UDI
Description: Probe Double End 15cm FDA UDI

Identifiers

Catalog Number: 26-106-16 FDA UDI
Primary DI / UDI-DI: 08403207004369 FDA UDI
FDA Product Code: MDM FDA UDI
GMDN Term: Neurosurgical probe 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 6 Inch FDA UDI

Category: Neurosurgical probe

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Anmuth Medical International Llc

Sources (1)

FDA UDI c3643634-7619-41a4-9197-2c16b2318e53 36 fields · synced May 30, 2026