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Wide Platform Implant Ca D:5.5 L:10

FDA UDI

Class II (US FDA UDI)

by Biotechnology Institute Sl

Identity

Trade Name
WIDE PLATFORM IMPLANT CA D:5.5 L:10 FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Model / Reference
IRPACA5510 FDA UDI

Identifiers

Primary DI / UDI-DI
08435389814931 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

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5.5 Millimeter FDA UDI
Length — 10 Millimeter FDA UDI

Category: Screw endosteal dental implant, two-piece

Wide Platform Implant Ca D:5.5 L:10 by Biotechnology Institute Sl — 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 cf29e6c0-3386-4426-8971-b86787559a65 34 fields · synced May 31, 2026