← Back to catalogue

Esophagus bougie diameter 10 mm, with bite protector and fixation

FDA UDI

Class II (US FDA UDI)

by Varian Medical Systems Deutschland GmbH

Identity

Trade Name
Esophagus bougie diameter 10 mm, with bite protector and fixation FDA UDI
Generic Name
Oesophagus brachytherapy system applicator, remote-afterloading FDA UDI
Model / Reference
GM11007420 FDA UDI

Identifiers

Catalog Number
GM11007420 FDA UDI
Primary DI / UDI-DI
00816389024151 FDA UDI
510(k) Number
K130251 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
Oesophagus 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 10 Millimeter FDA UDI

Category: Oesophagus brachytherapy system applicator, remote-afterloading

Esophagus bougie diameter 10 mm, with bite protector and fixation by Varian Medical Systems Deutschland GmbH — Class II — FDA UDI — listed in FDA GUDID

Similar devices

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

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 f62c722c-f1d1-4572-81df-4477c6ca30d0 35 fields · synced Jun 6, 2026