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Paddle/Condenser

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
PADDLE/CONDENSER FDA UDI
Generic Name
Dental amalgam condenser, reusable FDA UDI
Device Name
PADDLE/CONDENSER #3T DOUBLE ENDED FLARED/FLAT BLADES LIGHT HANDLE TITANIUM FDA UDI
Model / Reference
1102-REPFI3T FDA UDI
Description
PADDLE/CONDENSER #3T DOUBLE ENDED FLARED/FLAT BLADES LIGHT HANDLE TITANIUM FDA UDI

Identifiers

Catalog Number
1102-REPFI3T FDA UDI
Primary DI / UDI-DI
00192896088023 FDA UDI
FDA Product Code
EKG FDA UDI
GMDN Term
Dental amalgam condenser, 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

Category: Dental amalgam condenser, reusable

Paddle/Condenser by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental amalgam condenser, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 85088b42-3f3a-4edb-a577-57e6fa9ea89c 36 fields · synced Jun 8, 2026