← Back to catalogue

IPS e.max CAD

FDA UDI

Class II (US FDA UDI)

by Ivoclar Vivadent Aktiengesellschaft

Identity

Trade Name
IPS e.max CAD FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
CAD/CAM CS f. PrograMill Starter K. Rev1 FDA UDI
Model / Reference
748882AL FDA UDI
Description
CAD/CAM CS f. PrograMill Starter K. Rev1 FDA UDI

Identifiers

Catalog Number
748882AL FDA UDI
Primary DI / UDI-DI
DIVO748882AL1 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 FDA UDI
Commercial Distribution
Not 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

IPS e.max CAD by Ivoclar Vivadent Aktiengesellschaft — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 1d42d4a5-5cbf-4f44-810f-4e57ba85b55a 35 fields · synced May 31, 2026