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Dentapreg® SFU Reinforcement

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref D-505

by ADM, a.s.

Identity

Trade Name
Dentapreg® SFU Reinforcement EUDAMEDFDA UDI
Generic Name
Dental reinforcing fibre FDA UDI
Device Name
Dentapreg® SFU EUDAMED
Model / Reference
D-505 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08595652700320 EUDAMEDFDA UDI
Basic UDI-DI
85956527SFU9Z EUDAMED
510(k) Number
K952353 FDA UDI
FDA Product Code
EBF FDA UDI
EMDN Code
Q010199 CONSERVATIVE DENTISTRY AND ENDODONTICS 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

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

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® SFU Reinforcement 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 0a0ed2bd-cfa0-45d0-aeb2-a6ba9256e8db 61 fields · synced Jun 19, 2026
  • FDA UDI 774d364c-12b6-46bc-b58a-db2b7f3dd1f5 33 fields · synced May 30, 2026