← Back to catalogue

Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Endoscopic electrosurgical electrode, bipolar, reprocessed FDA UDI
Device Name
7209641 MICRO ABLATOR-S PRB,W/SUCTION FDA UDI
Model / Reference
7209641RH FDA UDI
Description
7209641 MICRO ABLATOR-S PRB,W/SUCTION FDA UDI

Identifiers

Catalog Number
7209641RH FDA UDI
Primary DI / UDI-DI
10888277375406 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, reprocessed 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

Yes

FDA UDI

Single Use

Yes

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

Category: Endoscopic electrosurgical electrode, monopolar, single-useEndoscopic electrosurgical electrode, bipolar, reprocessed

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, bipolar, reprocessed.

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
Medline Industries, Inc.

Sources (1)

  • FDA UDI f9645ff7-5e07-4000-b5a7-3eaaf0438568 35 fields · synced May 29, 2026