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Elastomeric Impression Material

FDA UDI

Class II (US FDA UDI)

by Shandong Huge Dental Material Corporation

Identity

Trade Name
Elastomeric Impression Material FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Model / Reference
Type 0 (Putty Hand-Mix) FDA UDI

Identifiers

Catalog Number
25g Catalyst * 50 FDA UDI
Primary DI / UDI-DI
06970402675059 FDA UDI
510(k) Number
K133071 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

Elastomeric Impression Material by Shandong Huge Dental Material Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6013a384-7887-4041-bde5-0488aba0ae4e 34 fields · synced Jun 6, 2026