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Dental Instrument

EUDAMEDFDA UDI

Class I (EU MDR)

Ref SDR001N

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
Digital Analog EUDAMED
Model / Reference
SDR001N EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08800016111279 EUDAMEDFDA UDI
Basic UDI-DI
B-08800016111279 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 27b8ecc6-4a1a-401b-9971-04bb8792837a 61 fields · synced Jul 14, 2026
  • FDA UDI 57fa893f-c8d1-4260-91ae-9185023261a7 32 fields · synced May 30, 2026