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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Rigid optical arthroscope, reusable FDA UDI
Device Name
SCOPE,SINUS,AUTOCLAVABLE,WIDE-ANGLE, FDA UDI
Model / Reference
MDG0207226 FDA UDI
Description
SCOPE,SINUS,AUTOCLAVABLE,WIDE-ANGLE, FDA UDI

Identifiers

Catalog Number
MDG0207226 FDA UDI
Primary DI / UDI-DI
10080196239726 FDA UDI
510(k) Number
K060233 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid optical arthroscope, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Over-the-Counter

Yes

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: Rigid optical arthroscope, reusable

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

Similar devices

Also classified as Rigid optical arthroscope, 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 3313bb83-f674-418b-b6c6-59891addcf19 36 fields · synced May 30, 2026