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microTargeting™ Microtable™ Platform – Single

FDA UDI

Class II (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
microTargeting™ Microtable™ Platform – Single FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Device Name
microTargeting(TM) Microtable(TM) Platform – Single FDA UDI
Model / Reference
66-MT-D1-00643 FDA UDI
Description
microTargeting(TM) Microtable(TM) Platform – Single FDA UDI

Identifiers

Catalog Number
66-MT-D1 FDA UDI
Primary DI / UDI-DI
00873263006436 FDA UDI
510(k) Number
K132611 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Neurological stereotactic surgery system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

microTargeting™ Microtable™ Platform – Single by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K132611 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fhc, Inc.

Sources (1)

  • FDA UDI e091963c-5f33-48fc-aa9c-dca7e48b7509 38 fields · synced May 31, 2026