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Prosthetic screw

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref J4005.1602

by ALTATEC GmbH

Identity

Trade Name
Prosthetic screw EUDAMED
Prosthetic screw, for bar abutment FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Prosthetic screw EUDAMED
J4005.1602 Prosthetic screw, for bar abutment, hex Ø 3.3/3.8/4.3 mm, thread M 1.6 FDA UDI
Model / Reference
J4005.1602 EUDAMEDFDA UDI
Description
J4005.1602 Prosthetic screw, for bar abutment, hex Ø 3.3/3.8/4.3 mm, thread M 1.6 FDA UDI

Identifiers

Catalog Number
J4005.1602 FDA UDI
Primary DI / UDI-DI
04099797004212 EUDAMED
E219J400516021 FDA UDI
Basic UDI-DI
40997970004501000000000HT EUDAMED
Secondary DI
E219J400516021 EUDAMED
FDA Product Code
NHA FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Prosthetic screw by ALTATEC GmbH — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ALTATEC GmbH
EUDAMED SRN
DE-MF-000006230

Sources (2)

  • EUDAMED f1c47ebe-3e8b-491c-9fff-694e84e426a0 61 fields · synced Jul 14, 2026
  • FDA UDI 1a573f19-823a-4aa1-a861-bd00558a151e 35 fields · synced May 30, 2026