Pricing Sign in

Role
Country
Date of registration
Address

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.

Organization name
UDI-DI code
Reference / catalog number

Total Etch Refill 2x2 g — Class IIa MDR by Ivoclar Vivadent AG

MD Atlas
Ivoclar Vivadent AG

EUDAMED last updated this device on Feb 6, 2026

Total Etch Refill 2x2 g

76152082AETCH001J9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ivoclar Vivadent AG
UDI-DI code: 07615208301472
Reference / catalog number: 550588AN

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?

View device family (Basic UDI)

Manufacturer information

Organization name: Ivoclar Vivadent AG
SRN: LI-MF-000000522
Manufacturer status: Active

Related devices

Adhese 100 Refill Bottle 1x6g76152082ABOND001HJOn the market Adhese 2 100 Refill Bottle 1x6g76152082ABOND010HKOn the market Adhese 2 Brush DC Endo blue 25 pcs76152082ABOND010HKOn the market Adhese 2 Brush DC Reg. blue 25 pcs76152082ABOND010HKOn the market Adhese 2 DC Ref. SD Sm/Endo 25x0.1g76152082ABOND010HKOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

No critical warnings reported for this device.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Liechtenstein; available across 1 country total.

Country	On market since	Until
LiechtensteinPrimary placement		Still on market

Device identification

Trade name: Total Etch Refill 2x2 g
UDI-DI code: 07615208301472
Basic UDI-DI: 76152082AETCH001J9
Reference / catalog number: 550588AN
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 2
Additional product description: Total Etch Refill 2x2 g
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q01010402ENAMEL-DENTINAL ETCHING MATERIALS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas