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

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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

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UDI-DI variants

392 UDI-DI variants

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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 BL2 C14/507615208367515
IPS e.max CAD CEREC/inLab HT BL2 C14/507615208549720
IPS e.max CAD CEREC/inLab HT BL2 I12/507615208367553
IPS e.max CAD CEREC/inLab HT BL3 C14/507615208549713
IPS e.max CAD CEREC/inLab HT BL3 C14/507615208367508
IPS e.max CAD CEREC/inLab HT BL3 I12/507615208367546
IPS e.max CAD CEREC/inLab HT BL4 C14/507615208367492
IPS e.max CAD CEREC/inLab HT BL4 I12/507615208367539
IPS e.max CAD CEREC/inLab HT C1 B40/307615208361520
IPS e.max CAD CEREC/inLab HT C1 B40L/307615208351415
IPS e.max CAD CEREC/inLab HT C1 C14/507615208367638
IPS e.max CAD CEREC/inLab HT C1 I12/507615208367799
IPS e.max CAD CEREC/inLab HT C2 B40/307615208361513
IPS e.max CAD CEREC/inLab HT C2 B40L/307615208351408
IPS e.max CAD CEREC/inLab HT C2 C14/507615208549751
IPS e.max CAD CEREC/inLab HT C2 C14/507615208367621
IPS e.max CAD CEREC/inLab HT C2 I12/507615208367782
IPS e.max CAD CEREC/inLab HT C3 C14/507615208367614
IPS e.max CAD CEREC/inLab HT C3 I12/507615208367775
IPS e.max CAD CEREC/inLab HT C4 C14/507615208367607
IPS e.max CAD CEREC/inLab HT C4 I12/507615208367768
IPS e.max CAD CEREC/inLab HT D2 B40/307615208361506
IPS e.max CAD CEREC/inLab HT D2 B40L/307615208351392
IPS e.max CAD CEREC/inLab HT D2 C14/507615208549744
IPS e.max CAD CEREC/inLab HT D2 C14/507615208367591

1 2 3 4 5

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