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Dentapreg® PFU Posterior Bridge

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref D-503

by ADM, a.s.

Identity

Trade Name
Dentapreg® PFU Posterior Bridge EUDAMEDFDA UDI
Generic Name
Dental reinforcing fibre FDA UDI
Device Name
Dentapreg® PFU EUDAMED
Model / Reference
D-503 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08595652700306 EUDAMEDFDA UDI
Basic UDI-DI
85956527PFU9J EUDAMED
510(k) Number
K952353 FDA UDI
FDA Product Code
EBF FDA UDI
EMDN Code
Q010299 PROSTHETIC DENTISTRY DEVICES - OTHER EUDAMED
GMDN Term
Dental reinforcing fibre FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Market of Registration
Czechia EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dentapreg® PFU Posterior Bridge by ADM, a.s. — 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
ADM, a.s.
EUDAMED SRN
CZ-MF-000032589

Sources (2)

  • EUDAMED 7033267a-717d-4213-a7f1-44f699872a5f 61 fields · synced Jul 20, 2026
  • FDA UDI a03b5adc-effb-44dc-af26-c5015640e15c 33 fields · synced May 30, 2026