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Guided Surgery Accessories KIT - RP&WP Implants

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref GSK004Model Kit_2

by Adin Dental Implant Systems LTD.

Identity

Trade Name
Guided Surgery Accessories KIT - RP&WP Implants EUDAMEDFDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Model / Reference
Kit_2 EUDAMED
GSK004 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
07290109302119 EUDAMEDFDA UDI
Basic UDI-DI
729010930FullKitKH EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L159016 DENTAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.3980 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

Guided Surgery Accessories KIT - RP&WP Implants by Adin Dental Implant Systems Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

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 cfc47f82-736d-4196-9072-b1bd91836cb9 61 fields · synced Jun 17, 2026
  • FDA UDI c5404d21-265d-4f29-a360-3d5954f7f233 32 fields · synced May 30, 2026