← Back to catalogue

Weropress

FDA UDI

Class II (US FDA UDI)

by Merz Dental GmbH

Identity

Trade Name
Weropress FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Weropress Polymer, BDLoad pink, 100g FDA UDI
Model / Reference
Weropress Polymer, BDLoad pink, 100g FDA UDI
Description
Weropress Polymer, BDLoad pink, 100g FDA UDI

Identifiers

Catalog Number
1025034 FDA UDI
Primary DI / UDI-DI
D7091025034 FDA UDI
510(k) Number
K130076 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Dental appliance fabrication material, resin

Weropress by Merz Dental GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Merz Dental GmbH

Sources (1)

  • FDA UDI 6daec604-0018-44b9-a5e2-684e8c2b34f7 36 fields · synced May 30, 2026