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Easy Bassi

FDA UDI

Class I (US FDA UDI)

by Easy Equipamentos Odontologicos Ltda.

Identity

Trade Name
Easy Bassi FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, single-use FDA UDI
Device Name
LIMA LOGIC SEQUENCE KIT2 15.10, 15.03, 20.05 & 35.05 21MM 4 UN FDA UDI
Model / Reference
BRKIT2LOGICS21BL FDA UDI
Description
LIMA LOGIC SEQUENCE KIT2 15.10, 15.03, 20.05 & 35.05 21MM 4 UN FDA UDI

Identifiers

Primary DI / UDI-DI
07908626202941 FDA UDI
FDA Product Code
EKS FDA UDI
GMDN Term
Rotary/reciprocating endodontic file/rasp, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rotary/reciprocating endodontic file/rasp, single-use

Easy Bassi by Easy Equipamentos Odontologicos Ltda. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rotary/reciprocating endodontic file/rasp, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82f83ae4-6d18-4a0c-bbe8-5f41538b2978 33 fields · synced May 30, 2026