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HEAT EXCHANGER SET (1 Piece)

FDA UDI

Class II (US FDA UDI)

by Belmont Instrument Corp.

Identity

Trade Name
HEAT EXCHANGER SET (1 Piece) FDA UDI
Generic Name
Extravascular-circulation hyperthermia system applicator, intracorporeal FDA UDI
Model / Reference
902-00006P FDA UDI

Identifiers

Primary DI / UDI-DI
00896128002145 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
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
MRI Safety
MR Unsafe FDA UDI

Category: Extravascular-circulation hyperthermia system applicator, intracorporeal

HEAT EXCHANGER SET (1 Piece) by Belmont Instrument Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extravascular-circulation hyperthermia system applicator, intracorporeal.

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 dc6542b3-d0f3-463f-9820-0bf884eb86a7 33 fields · synced Jun 8, 2026