← Back to catalogue

Delfin2

FDA UDI

Class I (US FDA UDI)

by Intra-Lock International

Identity

Trade Name
Delfin2 FDA UDI
Generic Name
Dental power tool system handpiece, line-powered FDA UDI
Device Name
Accessory, Pump Irrigation Tubing, 10 Pack (Single Use) FDA UDI
Model / Reference
DELF2-02 FDA UDI
Description
Accessory, Pump Irrigation Tubing, 10 Pack (Single Use) FDA UDI

Identifiers

Catalog Number
DELF2-02 FDA UDI
Primary DI / UDI-DI
D742DELF2020 FDA UDI
FDA Product Code
EKX FDA UDI
GMDN Term
Dental power tool system handpiece, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

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: Dental power tool system handpiece, line-powered

Delfin2 by Intra-Lock International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental power tool system handpiece, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 12110ccd-a79f-428b-808f-7980114e67b9 34 fields · synced May 30, 2026