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Prosthetic Kit Metal

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref PK6300Model Kit

by Adin Dental Implant Systems LTD.

Identity

Trade Name
Prosthetic Kit Metal EUDAMEDFDA UDI
Generic Name
Dental implant/prosthesis surgical procedure kit FDA UDI
Model / Reference
Kit EUDAMED
PK6300 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
07290105153661 EUDAMEDFDA UDI
Basic UDI-DI
729010515FullKitHE EUDAMED
FDA Product Code
DZN 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
872.4565 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

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

Prosthetic Kit Metal by Adin Dental Implant Systems 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
IL-MF-000014625
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (2)

  • EUDAMED 5f4b1c4f-cf4d-4dc3-ad77-8d0eeee99de1 61 fields · synced Jun 18, 2026
  • FDA UDI 7bc2d314-ef35-497f-833f-9e21c63529ce 32 fields · synced May 29, 2026