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Ipd

FDA UDI

Class I (US FDA UDI)

by Implant Protesis Dental 2004 Sl

Identity

Trade Name
IPD FDA UDI
Generic Name
Dental implant abutment analog, intraoral-scanning, single-use FDA UDI
Device Name
Scanflag - Jut Wing FDA UDI
Model / Reference
SC3D FDA UDI
Description
Scanflag - Jut Wing FDA UDI

Identifiers

Catalog Number
ROE/AB-SR-02/FS FDA UDI
Primary DI / UDI-DI
08435566643057 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment analog, intraoral-scanning, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant abutment analog, intraoral-scanning, single-use

Ipd by Implant Protesis Dental 2004 Sl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant abutment analog, intraoral-scanning, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5bdeb821-1712-4486-a7ba-bbb510a15959 35 fields · synced Jun 1, 2026