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AOS Universal Connecting Guide Tubes

FDA UDI

Class II (US FDA UDI)

by Alpha-Omega Services, Inc.

Identity

Trade Name
AOS Universal Connecting Guide Tubes FDA UDI
Generic Name
General-purpose brachytherapy system applicator, remote-afterloading FDA UDI
Device Name
Set, Universal Connecting Guide Tubes, Numbered, Series-15, 100 cm, Green Nylon, Set of 20 FDA UDI
Model / Reference
SGU0010-020 FDA UDI
Description
Set, Universal Connecting Guide Tubes, Numbered, Series-15, 100 cm, Green Nylon, Set of 20 FDA UDI

Identifiers

Primary DI / UDI-DI
00850645007557 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
General-purpose 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: General-purpose brachytherapy system applicator, remote-afterloading

AOS Universal Connecting Guide Tubes by Alpha-Omega Services, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose brachytherapy system applicator, remote-afterloading.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alpha-Omega Services, Inc.

Sources (1)

  • FDA UDI b0228f34-13c1-4e74-9540-ddb124772cc3 33 fields · synced Jun 8, 2026