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EDS Core Forms

FDA UDI

Class I (US FDA UDI)

by Essential Dental Systems, Inc.

Identity

Trade Name
EDS Core Forms FDA UDI
Generic Name
Dental mould FDA UDI
Device Name
48 Clear Core Forms FDA UDI
Model / Reference
890-00 FDA UDI
Description
48 Clear Core Forms FDA UDI

Identifiers

Catalog Number
890-00 FDA UDI
Primary DI / UDI-DI
00766054001294 FDA UDI
FDA Product Code
EIY FDA UDI
GMDN Term
Dental mould FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental mould

EDS Core Forms by Essential Dental Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mould.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d35ee18d-475f-42dd-9d83-92fdecfe7db8 35 fields · synced Jun 1, 2026