Septodont

FDA UDI

Class II (US FDA UDI)

by A.Titan Instruments

Identity

Trade Name: Septodont FDA UDI
Generic Name: Dental anaesthesia syringe, reusable FDA UDI
Device Name: Aspirating Syringe, Standard Thread, Medium, Stainless, Round Thumbring FDA UDI
Model / Reference: SE-6200 OR FDA UDI
Description: Aspirating Syringe, Standard Thread, Medium, Stainless, Round Thumbring FDA UDI

Identifiers

Primary DI / UDI-DI: 00841685104917 FDA UDI
FDA Product Code: EJI FDA UDI
GMDN Term: Dental anaesthesia syringe, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.6770 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Dry Heat Sterilization FDA UDI

Category: Dental anaesthesia syringe, reusable

Septodont by A.Titan Instruments — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: A.Titan Instruments

Sources (1)

FDA UDI d59853ed-3a60-4779-ac2b-fea47a34ab56 33 fields · synced Jun 9, 2026