← Back to catalogue

Straight In/Bifurcated Out Pt Line (1 Piece)

FDA UDI

Class II (US FDA UDI)

by Belmont Instrument Corp.

Identity

Trade Name
Straight In/Bifurcated Out Pt Line (1 Piece) FDA UDI
Generic Name
Extravascular-circulation hyperthermia system applicator, intracorporeal FDA UDI
Model / Reference
902-00040P FDA UDI

Identifiers

Primary DI / UDI-DI
00896128002152 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

Straight In/Bifurcated Out Pt Line (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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3b1a98d1-944f-44e3-97a4-45c75ee05a00 33 fields · synced May 31, 2026