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Hyperthermia Pump Y-Set Pt Line

FDA UDI

Class II (US FDA UDI)

by Belmont Instrument Corp.

Identity

Trade Name
Hyperthermia Pump Y-Set Pt Line FDA UDI
Generic Name
Extravascular-circulation hyperthermia system applicator, intracorporeal FDA UDI
Model / Reference
902-00004 FDA UDI

Identifiers

Primary DI / UDI-DI
10896128002265 FDA UDI
510(k) Number
K152208 FDA UDI
FDA Product Code
LGZ FDA UDI
GMDN Term
Extravascular-circulation hyperthermia system applicator, intracorporeal FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Hyperthermia Pump Y-Set Pt Line by Belmont Instrument Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cb91470c-ed56-442e-90b5-d58e4bb176c4 34 fields · synced Jun 1, 2026