Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

IPS e.max CAD — 392 UDI-DI variants, MDR (Ivoclar Vivadent AG)

MD Atlas
Ivoclar Vivadent AG

Data from EUDAMED, last updated May 31, 2026

IPS e.max CAD

76152082ACERA001EQ

392 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Ivoclar Vivadent AG

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

UDI-DI variants

392 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KKH4KVG4R71AHTM9EGS3C2SH

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

IPS e.max CAD CEREC/inLab HT D2 I12/507615208367751
IPS e.max CAD CEREC/inLab HT D3 C14/507615208367584
IPS e.max CAD CEREC/inLab HT D3 I12/507615208367744
IPS e.max CAD CEREC/inLab HT D4 C14/507615208367577
IPS e.max CAD CEREC/inLab HT D4 I12/507615208367737
IPS e.max CAD CEREC/inLab Imp. O1 C14/507615208360967
IPS e.max CAD CEREC/inLab Imp. O2 C14/507615208360950
IPS e.max CAD CEREC/inLab LT A1 B32/307615208351781
IPS e.max CAD CEREC/inLab LT A1 C14/507615208374629
IPS e.max CAD CEREC/inLab LT A1 C14/507615208298895
IPS e.max CAD CEREC/inLab LT A1 C14/507615208549942
IPS e.max CAD CEREC/inLab LT A1 C16/507615208351873
IPS e.max CAD CEREC/inLab LT A1 I12/507615208374711
IPS e.max CAD CEREC/inLab LT A1 I12/507615208298925
IPS e.max CAD CEREC/inLab LT A2 B32/307615208549690
IPS e.max CAD CEREC/inLab LT A2 B32/307615208296204
IPS e.max CAD CEREC/inLab LT A2 B32/307615208351774
IPS e.max CAD CEREC/inLab LT A2 C14/507615208374612
IPS e.max CAD CEREC/inLab LT A2 C14/507615208298888
IPS e.max CAD CEREC/inLab LT A2 C14/507615208549935
IPS e.max CAD CEREC/inLab LT A2 C16/507615208351866
IPS e.max CAD CEREC/inLab LT A2 I12/507615208550078
IPS e.max CAD CEREC/inLab LT A2 I12/507615208374704
IPS e.max CAD CEREC/inLab LT A2 I12/507615208298918
IPS e.max CAD CEREC/inLab LT A3 B32/307615208351767

2 3 4 5 6

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 76152082ACERA001EQ
Device name: IPS e.max CAD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ivoclar Vivadent AG
SRN: LI-MF-000000522
Country: Liechtenstein
Email: Sandro.Sbicego@ivoclar.com

Variants by status