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Conmed

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Rigid optical arthroscope, reusable FDA UDI
Device Name
AUTOCLAVABLE EYECUP SCOPE, 2.5 MM, 70° FDA UDI
Model / Reference
T2570 FDA UDI
Description
AUTOCLAVABLE EYECUP SCOPE, 2.5 MM, 70° FDA UDI

Identifiers

Catalog Number
T2570 FDA UDI
Primary DI / UDI-DI
10845854031858 FDA UDI
510(k) Number
K962075 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Rigid optical arthroscope, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.5 Millimeter FDA UDI
Angle — 70 degree FDA UDI

Category: Rigid optical arthroscope, reusable

Conmed by Conmed Corporation — 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

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 9ec648d4-9ad5-4ca0-82fe-b71f57a4df73 37 fields · synced May 30, 2026