← Back to catalogue

Prosthetic Accessories

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref D3N-3.75,9

by A.b. Dental Devices Ltd

Identity

Trade Name
Prosthetic Accessories FDA UDI
Generic Name
Dental implant suprastructure kit FDA UDI
Device Name
Class I - Dental Instruments EUDAMED
Narrow Clip Transfer FDA UDI
Model / Reference
D3N-3.75,9 EUDAMEDFDA UDI
Description
Narrow Clip Transfer FDA UDI

Identifiers

Catalog Number
D3N-3.75,9 FDA UDI
Primary DI / UDI-DI
07290107274531 EUDAMEDFDA UDI
Basic UDI-DI
729011127TOOLSClassI3T EUDAMED
510(k) Number
K132125 FDA UDI
FDA Product Code
NHA FDA UDI
EMDN Code
Q010599 DENTAL INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Dental implant suprastructure kit FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Poland 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure kit

Prosthetic Accessories by A.b. Dental Devices Ltd — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure kit.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (3)

  • FDA UDI 552955b8-4f6e-41d4-970f-6ddff5bf7401 36 fields · synced Jul 9, 2026
  • EUDAMED 5fc449ba-eab5-4503-b516-4f027adf59cc-1 61 fields · synced Jul 9, 2026
  • EUDAMED 5fc449ba-eab5-4503-b516-4f027adf59cc-2 61 fields · synced Jul 9, 2026