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5 ParaPost Fiber Lux Posts (.036" / 0.90mm)

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref PF1713

by Coltene/Whaledent Inc.

Identity

Trade Name
5 ParaPost Fiber Lux Posts (.036" / 0.90mm) EUDAMED
ParaPost Fiber Lux FDA UDI
Generic Name
Root canal post, preformed FDA UDI
Device Name
ParaPost Fiber Lux EUDAMED
5 ParaPost FiberLux Posts, Size 3 FDA UDI
Model / Reference
PF1713 EUDAMEDFDA UDI
Description
5 ParaPost FiberLux Posts, Size 3 FDA UDI

Identifiers

Primary DI / UDI-DI
D661PF17131 EUDAMEDFDA UDI
Basic UDI-DI
B-D661PF17131 EUDAMED
FDA Product Code
ELR FDA UDI
EMDN Code
Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED
GMDN Term
Root canal post, preformed FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.3810 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental appliance fabrication material, ceramic

5 ParaPost Fiber Lux Posts (.036" / 0.90mm) by Coltene/Whaledent Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000015761
Authorised Representative
Coltène/Whaledent GmbH + Co. KG DE-AR-000005719

Sources (2)

  • EUDAMED 0c47f4ea-e3f2-4f4d-8217-5961e396f3ae 61 fields · synced Jun 18, 2026
  • FDA UDI 4813608c-22ad-4a31-b3f5-a13ecfa4ed03 33 fields · synced May 30, 2026