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Dental Instrument

EUDAMEDFDA UDI

Class I (EU MDR)

Ref AMCL001

by Cowellmedi Co., Ltd.

Identity

Trade Name
Dental Instrument EUDAMED
Mini Plus Implant System FDA UDI
Generic Name
Screw endosteal dental implant, one-piece FDA UDI
Device Name
Lab Analog(Cemented type) EUDAMED
Model / Reference
AMCL001 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08809471729678 EUDAMEDFDA UDI
Basic UDI-DI
B-08809471729678 EUDAMED
510(k) Number
K090049 FDA UDI
FDA Product Code
DZE FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Screw endosteal dental implant, one-piece FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

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 7c441da9-2e98-4243-9271-98b8d140400b 61 fields · synced May 29, 2026
  • FDA UDI 0bce50e5-0616-435d-8e08-2d62b5171d2c 33 fields · synced May 27, 2026