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Thermique™

FDA UDI

Class II (US FDA UDI)

by Parkell, Inc.

Identity

Trade Name
Thermique™ FDA UDI
Generic Name
Endodontic obturation system FDA UDI
Device Name
Fine Thermique™ Condenser Tip FDA UDI
Model / Reference
D531 FDA UDI
Description
Fine Thermique™ Condenser Tip FDA UDI

Identifiers

Catalog Number
D531 FDA UDI
Primary DI / UDI-DI
M595D5310 FDA UDI
FDA Product Code
EAT FDA UDI
GMDN Term
Endodontic obturation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1720 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

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

Thermique™ by Parkell, Inc. — 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

Manufacturer
Parkell, Inc.

Sources (1)

  • FDA UDI 78904e5a-7585-4786-b06d-7f94c9748041 36 fields · synced May 31, 2026