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SR Ivocap High Impact

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 629288AN

by Ivoclar Vivadent Aktiengesellschaft

Identity

Trade Name
SR Ivocap HI Standard Kit Pref. Implant EUDAMED
SR Ivocap High Impact FDA UDI
Generic Name
Denture base resin kit FDA UDI
Device Name
IvoBase Hybrid, SR Ivocap High Impact, SR Ivocap Clear, SR Triplex Hot/SR Triplex Cold EUDAMED
SR Ivocap HI Standard Kit Pref. Implant FDA UDI
Model / Reference
629288AN EUDAMEDFDA UDI
Description
SR Ivocap HI Standard Kit Pref. Implant FDA UDI

Identifiers

Catalog Number
629288AN FDA UDI
Primary DI / UDI-DI
07615208297447 EUDAMEDFDA UDI
Basic UDI-DI
76152082APROS009WB EUDAMED
FDA Product Code
EBI FDA UDI
EMDN Code
Q010699 MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER EUDAMED
GMDN Term
Denture base resin kit FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Market of Registration
Liechtenstein EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Category: Denture base resin kit

SR Ivocap High Impact by Ivoclar Vivadent Aktiengesellschaft — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Denture base resin kit.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 71dbde3c-6879-419d-92e3-df3acd24134d 34 fields · synced Aug 2, 2026
  • EUDAMED 35d78943-1e92-46fc-aafd-3da05a4d2cbb 61 fields · synced Aug 2, 2026