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Quickcheck

FDA UDI

Class II (US FDA UDI)

by PTW-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH

Identity

Trade Name
QUICKCHECK FDA UDI
Generic Name
Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI
Model / Reference
QUICKCHECK webline FDA UDI

Identifiers

Catalog Number
T42031 FDA UDI
Primary DI / UDI-DI
EPTWT420310 FDA UDI
510(k) Number
K972211 FDA UDI
FDA Product Code
LHN FDA UDI
GMDN Term
Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-modality therapeutic radiation phantom, anthropomorphic

Quickcheck by PTW-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality therapeutic radiation phantom, anthropomorphic.

Cleared under the same submission

K972211 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PTW-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH

Sources (1)

  • FDA UDI e42979e7-5b68-4aba-95a4-bf383c198e28 34 fields · synced Jun 9, 2026