← Back to catalogue

PDT, Inc.

FDA UDI

Class I (US FDA UDI)

by PDT, Inc.

Identity

Trade Name
PDT, Inc. FDA UDI
Generic Name
Dental amalgam condenser, reusable FDA UDI
Device Name
Blacks Plugger 1/2 Serrated FDA UDI
Model / Reference
R348S Blacks Plugger 1/2 Serrated FDA UDI
Description
Blacks Plugger 1/2 Serrated FDA UDI

Identifiers

Catalog Number
R348S FDA UDI
Primary DI / UDI-DI
00813677021854 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

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

Yes

FDA UDI

Lot / Batch Number

No

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 Conditional FDA UDI

Category: Dental amalgam condenser, reusable

PDT, Inc. by PDT, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
PDT, Inc.

Sources (1)

  • FDA UDI fa300ff6-d2c1-4b49-ba94-6700166a74dc 34 fields · synced Jun 9, 2026