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Contour Meniscus Arrow

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONTOUR MENISCUS ARROW FDA UDI
Generic Name
Meniscus screw FDA UDI
Device Name
CONTOUR MENISCUS ARROW SELF-REINFORCED TECHNOLOGY Ø1.1 X 13 MM FDA UDI
Model / Reference
541113 FDA UDI
Description
CONTOUR MENISCUS ARROW SELF-REINFORCED TECHNOLOGY Ø1.1 X 13 MM FDA UDI

Identifiers

Catalog Number
541113 FDA UDI
Primary DI / UDI-DI
20845854040147 FDA UDI
FDA Product Code
MAI FDA UDI
GMDN Term
Meniscus screw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 1.1 Millimeter FDA UDI
Length — 13 Millimeter FDA UDI

Category: Meniscus screw

Contour Meniscus Arrow by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Meniscus screw.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 87c8b99b-fe08-4453-8d2e-6289a97a4686 37 fields · synced Jun 6, 2026