Elipar™ DeepCure-S

FDA UDI

Class II (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name: Elipar™ DeepCure-S FDA UDI
Generic Name: Dental laboratory curing unit FDA UDI
Device Name: 3M™ ESPE™ Elipar™ DeepCure-S Light Guide, 10mm, 76981 FDA UDI
Model / Reference: 76981 FDA UDI
Description: 3M™ ESPE™ Elipar™ DeepCure-S Light Guide, 10mm, 76981 FDA UDI

Identifiers

Catalog Number: 76981 FDA UDI
Primary DI / UDI-DI: J001702011441470 FDA UDI
FDA Product Code: EBZ FDA UDI
GMDN Term: Dental laboratory curing unit FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.6070 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 10 Millimeter FDA UDI

Category: Dental laboratory curing unit

Elipar™ DeepCure-S by 3M Deutschland GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: 3M Deutschland GmbH

Sources (1)

FDA UDI ca1c54d7-b3fe-4c04-9c7f-1ad6b9b90e35 36 fields · synced May 30, 2026