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Quala

FDA UDI

Class II (US FDA UDI)

by National Distribution & Contracting, Inc.

Identity

Trade Name
Quala FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Quala HP Bite Registration Reg Set FDA UDI
Model / Reference
Q-9001HP FDA UDI
Description
Quala HP Bite Registration Reg Set FDA UDI

Identifiers

Catalog Number
Q-9001HP FDA UDI
Primary DI / UDI-DI
D023Q9001HP0 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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

Yes

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: Silicone dental impression material

Quala by National Distribution & Contracting, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22a766b5-f421-4a36-8ce6-625f8f7a541d 35 fields · synced Jun 1, 2026