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Astra Tech Implant System® EV

FDA UDI

Class II (US FDA UDI)

by Dentsply Implants Manufacturing GmbH

Identity

Trade Name
Astra Tech Implant System® EV FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Astra Tech Implant EV Profile 4.2 PS - 13 mm OsseoSpeed® FDA UDI
Model / Reference
26374 FDA UDI
Description
Astra Tech Implant EV Profile 4.2 PS - 13 mm OsseoSpeed® FDA UDI

Identifiers

Catalog Number
26374 FDA UDI
Primary DI / UDI-DI
07392532214615 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, two-piece 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Screw endosteal dental implant, two-piece

Astra Tech Implant System® EV by Dentsply Implants Manufacturing GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screw endosteal dental implant, two-piece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI df23e331-e62c-4432-9726-386cc2dc41bd 36 fields · synced May 31, 2026