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Final Abutment: Variobase C

EUDAMEDFDA UDIFDA 510(k)

Class IIb (EU MDR)

Ref 062.4982

by Institut Straumann AG

Identity

Trade Name
Variobase C FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Final Abutment: Variobase C EUDAMED
Implantborne Elements FDA UDI
Model / Reference
062.4982 EUDAMED
RB/WB Variobase C, Ø4.5, GH 1.5, TAN FDA UDI
Description
Implantborne Elements FDA UDI

Identifiers

Catalog Number
062.4982 FDA UDI
Primary DI / UDI-DI
07630031747051 EUDAMEDFDA UDI
Basic UDI-DI
0763003170074QX EUDAMED
510(k) Number
K192742 FDA UDI
FDA Product Code
NHA FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Final Abutment: Variobase C by Institut Straumann AG — Class IIb — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Institut Straumann AG
EUDAMED SRN
CH-MF-000009933
Authorised Representative
Etkon GmbH DE-AR-000009335

Sources (3)

  • EUDAMED 5513e612-6601-41f3-82a5-ca972db4bad4 61 fields · synced Jul 15, 2026
  • FDA UDI fc363c6a-fb05-4577-9ed4-a34fa41fe3f0 36 fields · synced May 30, 2026
  • FDA 510(k) K192742 1 fields · synced May 18, 2026