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Epitech

FDA UDI

Class I (US FDA UDI)

by Tara Medical Devices Llc

Identity

Trade Name
EPITECH FDA UDI
Generic Name
Dermatome handpiece, electrically-powered FDA UDI
Device Name
EPITECH 1002 Chamber, Six Orifice, Single Use FDA UDI
Model / Reference
1002 FDA UDI
Description
EPITECH 1002 Chamber, Six Orifice, Single Use FDA UDI

Identifiers

Catalog Number
CH1002A-6 FDA UDI
Primary DI / UDI-DI
G021CH1002A60 FDA UDI
FDA Product Code
GFD FDA UDI
GMDN Term
Dermatome handpiece, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Liquid Chemical FDA UDI

Category: Dermatome handpiece, electrically-powered

Epitech by Tara Medical Devices Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatome handpiece, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tara Medical Devices Llc

Sources (1)

  • FDA UDI 35243d67-6bf5-4baa-a2e5-708d2a1c532d 36 fields · synced May 30, 2026