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Ultra Safety Plus Twist Reusable Handle

FDA UDI

Class II (US FDA UDI)

by Septodont Sas Specialites Septodont

Identity

Trade Name
Ultra Safety Plus Twist Reusable Handle FDA UDI
Generic Name
Dental anaesthesia syringe, reusable FDA UDI
Device Name
1 handle to be sterilized FDA UDI
Model / Reference
01N3200 FDA UDI
Description
1 handle to be sterilized FDA UDI

Identifiers

Primary DI / UDI-DI
03701398103232 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
Not 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

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
Moist Heat or Steam Sterilization FDA UDI

Ultra Safety Plus Twist Reusable Handle by Septodont Sas Specialites Septodont — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0726e104-2841-459f-9b03-d17718f047c5 34 fields · synced Jun 6, 2026