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Conmed

EUDAMEDFDA UDI

Class IIa (EU MDD (legacy))

Ref 5023-186

by Conmed Corporation

Identity

Trade Name
CONMED EUDAMEDFDA UDI
Generic Name
ARTHROSCOPY BLADES, SINGLE-USE EUDAMED
Surgical saw blade, sagittal, single-use FDA UDI
Device Name
Orthopedic, Non-active, Handpiece Blade, Sagittal EUDAMED
MICRO CHOICE ACL BLADE, 8.5 X 38 X 0.4 MM FDA UDI
Model / Reference
5023-186 EUDAMED
00502318600 FDA UDI
Description
MICRO CHOICE ACL BLADE, 8.5 X 38 X 0.4 MM FDA UDI

Identifiers

Catalog Number
5023-186 FDA UDI
Primary DI / UDI-DI
10845854002209 EUDAMEDFDA UDI
Basic UDI-DI
B-10845854002209 EUDAMED
FDA Product Code
GFA FDA UDI
EMDN Code
K030203 ARTHROSCOPY BLADES, SINGLE-USE EUDAMED
GMDN Term
Surgical saw blade, sagittal, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Legislation / Framework
MDD (Directive 93/42/EEC on Medical Devices) EUDAMED
Regulation Number
878.4820 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

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
Width — 8.5 Millimeter FDA UDI
Length — 38 Millimeter FDA UDI
Height — 0.4 Millimeter FDA UDI

Conmed by Conmed Corporation (arthroscopy blades, single-use) — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation
EUDAMED SRN
US-MF-000012663
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 68 fields · synced May 30, 2026
  • FDA UDI d968b07f-7537-4285-963b-7ba56029e1aa 36 fields · synced May 30, 2026