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Acculan 3ti

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
ACCULAN 3TI FDA UDI
Generic Name
Dermatome handpiece, electrically-powered FDA UDI
Device Name
Acculan 3Ti dermatome FDA UDI
Model / Reference
GA670 FDA UDI
Description
Acculan 3Ti dermatome FDA UDI

Identifiers

Catalog Number
GA670 FDA UDI
Primary DI / UDI-DI
04046963406196 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

No

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

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

Category: Dermatome handpiece, electrically-powered

Acculan 3ti by Aesculap, Inc. — 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
Aesculap, Inc.

Sources (1)

  • FDA UDI aedda0a6-3a99-43bc-b628-29a6c373331b 35 fields · synced Jun 1, 2026