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NanoPaq A 1, 4 g

FDA UDI

Class II (US FDA UDI)

by Schütz Dental GmbH

Identity

Trade Name
NanoPaq A 1, 4 g FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
NanoPaq is a light-curing nano-composite for the adhesive filling technique. It contains an ultrafine, radiopaque glass filler. FDA UDI
Model / Reference
234510 FDA UDI
Description
NanoPaq is a light-curing nano-composite for the adhesive filling technique. It contains an ultrafine, radiopaque glass filler. FDA UDI

Identifiers

Primary DI / UDI-DI
ESDG2345101 FDA UDI
FDA Product Code
EMA FDA UDI
EBC FDA UDI
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
872.3765 FDA UDI
872.3690 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental composite resin

NanoPaq A 1, 4 g by Schütz Dental GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Schütz Dental GmbH

Sources (1)

  • FDA UDI ee3b96eb-4d4c-4d76-ad43-9ab91b026b8f 34 fields · synced Jun 8, 2026