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Pro-Paks

FDA UDI

Class I (US FDA UDI)

by Microspecialities, Inc.

Identity

Trade Name
Pro-Paks FDA UDI
Generic Name
Skin marking guide, single-use FDA UDI
Device Name
Fine Tip Marking Pen Genian Violet, 20/bx. Our surgical marking pens contain a large reservoir if medical grade non-irrating gentian violet ink. FDA UDI
Model / Reference
MK-9002 FDA UDI
Description
Fine Tip Marking Pen Genian Violet, 20/bx. Our surgical marking pens contain a large reservoir if medical grade non-irrating gentian violet ink. FDA UDI

Identifiers

Catalog Number
MK-9002 FDA UDI
Primary DI / UDI-DI
10810003223446 FDA UDI
FDA Product Code
HMR FDA UDI
GMDN Term
Skin marking guide, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4570 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

Yes

FDA UDI

Category: Skin marking guide, single-use

Pro-Paks by Microspecialities, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin marking guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 78a0e328-40a8-4ce0-b4dc-d15024f1d968 35 fields · synced Jun 1, 2026