← Back to catalogue

Bonascan Heavy

FDA UDI

Class II (US FDA UDI)

by Dmp Dental Industry S.a.

Identity

Trade Name
BONASCAN HEAVY FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Addition curing vinyl polysiloxane scannable impression material FDA UDI
Model / Reference
Regular Set, 50ml FDA UDI
Description
Addition curing vinyl polysiloxane scannable impression material FDA UDI

Identifiers

Primary DI / UDI-DI
05206569000764 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

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: Silicone dental impression material

Bonascan Heavy by Dmp Dental Industry S.a. — 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

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

Manufacturer

Sources (1)

  • FDA UDI 06e896c5-1a9d-46fd-9ccc-3d664f69582c 35 fields · synced May 31, 2026