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Interna® Universal Platform Implant Ø4, 25 ↕7, 5

FDA UDI

Class II (US FDA UDI)

by Biotechnology Institute Sl

Identity

Trade Name
INTERNA® UNIVERSAL PLATFORM IMPLANT Ø4,25 ↕7,5 FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Model / Reference
IIPU4275 FDA UDI

Identifiers

Primary DI / UDI-DI
08435389808275 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
Not 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 — 4.25 Millimeter FDA UDI
Length — 7.5 Millimeter FDA UDI

Interna® Universal Platform Implant Ø4, 25 ↕7, 5 by Biotechnology Institute Sl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biotechnology Institute Sl

Sources (1)

  • FDA UDI 332985e5-a360-4c36-a7df-c071fad7f9e2 35 fields · synced May 31, 2026