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Bronchial catheter, ø 1.84 mm, sterile

FDA UDI

Class II (US FDA UDI)

by Varian Medical Systems, Inc

Identity

Trade Name
Bronchial catheter, ø 1.84 mm, sterile FDA UDI
Generic Name
Bronchial brachytherapy system applicator, remote-afterloading FDA UDI
Model / Reference
GM11002260 FDA UDI

Identifiers

Catalog Number
GM11002260 FDA UDI
Primary DI / UDI-DI
00816389028319 FDA UDI
510(k) Number
K082653 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
Bronchial 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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 Safe FDA UDI

Category: Bronchial brachytherapy system applicator, remote-afterloading

Bronchial catheter, ø 1.84 mm, sterile by Varian Medical Systems, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bronchial brachytherapy system applicator, remote-afterloading.

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 f7c7c278-d40a-46bc-92af-f7be62c4e2cd 34 fields · synced May 30, 2026