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Delasco Bipolar Forceps

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name
Delasco Bipolar Forceps FDA UDI
Generic Name
Endoscopic electrosurgical electrode, bipolar, reusable FDA UDI
Device Name
FORCEPS,BIPOLAR,CUSHING 7inSTRGHT, 1.0MM SMOOTH. Medical Device. FDA UDI
Model / Reference
26405 FDA UDI
Description
FORCEPS,BIPOLAR,CUSHING 7inSTRGHT, 1.0MM SMOOTH. Medical Device. FDA UDI

Identifiers

Catalog Number
26405 FDA UDI
Primary DI / UDI-DI
00609960000466 FDA UDI
510(k) Number
K964176 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, reusable 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscopic electrosurgical electrode, bipolar, reusable

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

Similar devices

Also classified as Endoscopic electrosurgical electrode, bipolar, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2b564412-6d2c-4d55-8537-fd0bf7014349 35 fields · synced May 30, 2026