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Stabident

FDA UDI

Class I (US FDA UDI)

by Fairfax Medical Products Limited

Identity

Trade Name
Stabident FDA UDI
Generic Name
Dental anaesthesia injection kit FDA UDI
Device Name
Dental anaesthesia injection kit FDA UDI
Model / Reference
Stabident Standard kit FDA UDI
Description
Dental anaesthesia injection kit FDA UDI

Identifiers

Catalog Number
ST FDA UDI
Primary DI / UDI-DI
05060489370136 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Dental anaesthesia injection kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental anaesthesia injection kit

Stabident by Fairfax Medical Products Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental anaesthesia injection kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cf7dcd8a-2d68-49bc-88f4-70cfd22fe47d 35 fields · synced May 30, 2026