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Microtek

FDA UDI

Class II (US FDA UDI)

by Microtek Medical LLC

Identity

Trade Name
MICROTEK FDA UDI
Generic Name
Dermatological solid-state laser system FDA UDI
Device Name
ANGIO DRAPE - INTRAJUGULAR/SUBCLAVIAN, 1-EACH FDA UDI
Model / Reference
1 FDA UDI
Description
ANGIO DRAPE - INTRAJUGULAR/SUBCLAVIAN, 1-EACH FDA UDI

Identifiers

Primary DI / UDI-DI
00748426077168 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Dermatological solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

No

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Dermatological solid-state laser system

Microtek by Microtek Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological solid-state laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microtek Medical LLC

Sources (1)

  • FDA UDI cfcc3943-99f7-42b4-90e7-d7f6d667d900 35 fields · synced Jun 8, 2026