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MUPIT Applicator

FDA UDI

Class II (US FDA UDI)

by Nucletron B.V.

Identity

Trade Name
MUPIT Applicator FDA UDI
Generic Name
General-purpose brachytherapy system applicator, remote-afterloading FDA UDI
Device Name
MUPIT Applicator Set 1.9mm FDA UDI
Model / Reference
083571P01-03 FDA UDI
Description
MUPIT Applicator Set 1.9mm FDA UDI

Identifiers

Primary DI / UDI-DI
08717213051355 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
General-purpose brachytherapy system applicator, remote-afterloading FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5700 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: General-purpose brachytherapy system applicator, remote-afterloading

MUPIT Applicator by Nucletron B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose brachytherapy system applicator, remote-afterloading.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nucletron B.V.

Sources (1)

  • FDA UDI f65024ff-0209-482b-aaac-13de7b8c14d2 35 fields · synced May 30, 2026