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Dental Instrument

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ILSR070

by Cowellmedi Co., Ltd.

Identity

Trade Name
Dental Instrument EUDAMED
Dental Implants Accesseories-Reusable FDA UDI
Generic Name
Dental implant abutment analog, laboratory FDA UDI
Device Name
Solid Lab Analog EUDAMED
Model / Reference
ILSR070 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08809471727476 EUDAMEDFDA UDI
Basic UDI-DI
B-08809471727476 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant abutment analog, laboratory FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dental Instrument by Cowellmedi Co., Ltd — Class I — 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

EUDAMED SRN
KR-MF-000009689
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (2)

  • EUDAMED 75d1344c-376b-486c-b39c-3ca7a52edab0 61 fields · synced Jun 6, 2026
  • FDA UDI 2ba9eec2-ccb9-407d-9664-e7df499462c2 32 fields · synced May 30, 2026