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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 handpiece/electrode, bipolar, reprocessed FDA UDI
Device Name
AC 1336-01 LO-PRO 90 DEGREE ARTHROW,W FDA UDI
Model / Reference
AC133601RH FDA UDI
Description
AC 1336-01 LO-PRO 90 DEGREE ARTHROW,W FDA UDI

Identifiers

Catalog Number
AC133601RH FDA UDI
Primary DI / UDI-DI
10080196385331 FDA UDI
510(k) Number
K171324 FDA UDI
FDA Product Code
NUJ FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/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 handpiece/electrode, bipolar, reprocessedEndoscopic 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 b26c2375-6af0-43ee-8cc5-058b4622564d 36 fields · synced May 30, 2026