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Allon®

FDA UDI

Class II (US FDA UDI)

by Belmont Instrument Corp.

Identity

Trade Name
Allon® FDA UDI
Generic Name
External circulating-fluid core temperature regulation system control unit, heating/cooling FDA UDI
Model / Reference
200-00263 FDA UDI

Identifiers

Catalog Number
200-00263 FDA UDI
Primary DI / UDI-DI
07290107581103 FDA UDI
FDA Product Code
DWJ FDA UDI
GMDN Term
External circulating-fluid core temperature regulation system control unit, heating/cooling FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5900 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: External circulating-fluid core temperature regulation system control unit, heating/cooling

Allon® by Belmont Instrument Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External circulating-fluid core temperature regulation system control unit, heating/cooling.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5c1fd84-b469-41cb-b399-5694b7622b09 34 fields · synced Jun 6, 2026