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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, Petite Blue Metric SEPTODONT LOGO CE MARK FDA UDI
Model / Reference
SE-7410 FDA UDI
Description
Aspirating Syringe, Petite Blue Metric SEPTODONT LOGO CE MARK FDA UDI

Identifiers

Primary DI / UDI-DI
00841685103941 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

No

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

Similar devices

Also classified as Dental anaesthesia syringe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A.Titan Instruments

Sources (1)

  • FDA UDI aa1de381-6840-430e-acb5-e4ecacc4ed09 33 fields · synced Jun 9, 2026