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Emiluma

FDA UDI

Class I (US FDA UDI)

by Ultradent Products, Inc.

Identity

Trade Name
Emiluma FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Emiluma Refill Kit 2 pk FDA UDI
Model / Reference
500081 FDA UDI
Description
Emiluma Refill Kit 2 pk FDA UDI

Identifiers

Catalog Number
500081 FDA UDI
Primary DI / UDI-DI
00883205032072 FDA UDI
FDA Product Code
EBH FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3670 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

Yes

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

Emiluma by Ultradent Products, Inc. — Class I — 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 a6729317-1915-4eeb-ada3-f28888ebb61d 36 fields · synced Jun 8, 2026