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Azure

FDA UDI

Class II (US FDA UDI)

by Terrats Medical Sl.

Identity

Trade Name
Azure FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
Conical BL FDA UDI
Model / Reference
IBL1480080 FDA UDI
Description
Conical BL FDA UDI

Identifiers

Catalog Number
AITBL-IMP4808 FDA UDI
Primary DI / UDI-DI
08435750409612 FDA UDI
510(k) Number
K212538 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental implant system

Azure by Terrats Medical Sl. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terrats Medical Sl.

Sources (1)

  • FDA UDI 05287854-3bea-4a85-91d8-1aa1b719ed32 36 fields · synced May 31, 2026