Pmt Corporation

FDA UDI

Class II (US FDA UDI)

by Pmt Corp.

Identity

Trade Name: PMT CORPORATION FDA UDI
Generic Name: Neurological stereotactic surgery system FDA UDI
Device Name: AUTOGUIDE BUSHING, 2.2MM DRILL, DRIVER FDA UDI
Model / Reference: 2103-221 FDA UDI
Description: AUTOGUIDE BUSHING, 2.2MM DRILL, DRIVER FDA UDI

Identifiers

Primary DI / UDI-DI: 00650551002673 FDA UDI
FDA Product Code: IKD FDA UDI
GMDN Term: Neurological stereotactic surgery system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.1175 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Hydrogen Peroxide FDA UDI

Category: Neurological stereotactic surgery system

Pmt Corporation by Pmt Corp. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Pmt Corp.

Sources (1)

FDA UDI 5d60980c-fc24-4801-99c9-c9c45c189dc8 33 fields · synced May 30, 2026