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Dispenser

FDA UDI

Class I (US FDA UDI)

by Vannini Dental Industry Srl

Identity

Trade Name
DISPENSER FDA UDI
Generic Name
Dental impression material syringe, reusable FDA UDI
Device Name
Dispenser for A-silicones FDA UDI
Model / Reference
051030 FDA UDI
Description
Dispenser for A-silicones FDA UDI

Identifiers

Catalog Number
051030 FDA UDI
Primary DI / UDI-DI
08033712562858 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Dental impression material syringe, reusable 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

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

Yes

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
MRI Safety
MR Safe FDA UDI

Category: Dental impression material syringe, reusable

Dispenser by Vannini Dental Industry Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental impression material syringe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11a329c8-cc6b-4a3a-9885-c671a19e618d 35 fields · synced Jun 1, 2026