← Back to catalogue

Delasco 734 Handpiece

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name
Delasco 734 Handpiece FDA UDI
Generic Name
Electrosurgical system generator FDA UDI
Device Name
HANDPIECE, REPLACEMENT FOR 734 & 1134 FDA UDI
Model / Reference
734/H FDA UDI
Description
HANDPIECE, REPLACEMENT FOR 734 & 1134 FDA UDI

Identifiers

Primary DI / UDI-DI
00609960000190 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrosurgical system generator

Delasco 734 Handpiece by Dermatologic Lab And Supply, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dermatologic Lab And Supply, Inc.

Sources (1)

  • FDA UDI 92aceb5e-ac19-41d9-974c-728b25225eba 33 fields · synced Jun 6, 2026