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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
72202139 DYONICS RF-S WHIRLWIND 90 PRB, FDA UDI
Model / Reference
72202139RH FDA UDI
Description
72202139 DYONICS RF-S WHIRLWIND 90 PRB, FDA UDI

Identifiers

Catalog Number
72202139RH FDA UDI
Primary DI / UDI-DI
10888277681477 FDA UDI
510(k) Number
K171324 FDA UDI
FDA Product Code
NUJ 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, 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.

Cleared under the same submission

K171324 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 09b0333b-b2cd-43c1-a1c2-0e86ec532f90 36 fields · synced Jun 7, 2026