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microTargeting™ Stylet

FDA UDI

Class I (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
microTargeting™ Stylet FDA UDI
Generic Name
Scalpel, single-use FDA UDI
Device Name
microTargeting DP Stylet, 1x, for use with mT Drive and STar Drive FDA UDI
Model / Reference
66-ST-14P-00822 FDA UDI
Description
microTargeting DP Stylet, 1x, for use with mT Drive and STar Drive FDA UDI

Identifiers

Catalog Number
66-ST-14P FDA UDI
Primary DI / UDI-DI
00873263008225 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Scalpel, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 1.83 Millimeter FDA UDI
Length — 204 Millimeter FDA UDI

Category: Scalpel, single-use

microTargeting™ Stylet by Fhc, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalpel, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fhc, Inc.

Sources (1)

  • FDA UDI abc399a5-4dc1-4301-b710-0f2e44e9353e 37 fields · synced May 30, 2026