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Karbp3000

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref KARBP3000

by MegaGen Implant Co., Ltd.

Identity

Trade Name
Bone Profiler Kit FDA UDI
Generic Name
Dental implant/prosthesis surgical procedure kit FDA UDI
Device Name
AnyRidge Internal FDA UDI
Model / Reference
KARBP3000 EUDAMEDFDA UDI
Description
AnyRidge Internal FDA UDI

Identifiers

Catalog Number
KARBP3000 FDA UDI
Primary DI / UDI-DI
08806388224630 EUDAMEDFDA UDI
Basic UDI-DI
880972899232P EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L159016 DENTAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
GMDN Term
Dental implant/prosthesis surgical procedure kit FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Karbp3000 by Megagen Implant Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/maxillofacial surgical procedure kit, non-medicated, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
KR-MF-000009885
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 7a5004b6-6e4d-4026-90ea-12a6ea28e2ca 61 fields · synced Jul 30, 2026
  • FDA UDI d52e232e-f887-4d40-93b3-53fa7ae54fdd 34 fields · synced May 30, 2026