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Prostate Stabilization Set

FDA UDI

Class I (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Prostate Stabilization Set FDA UDI
Generic Name
Prostate brachytherapy system applicator, manual FDA UDI
Device Name
Echker & Ziegler Prostate Stabilization Set 18ga x 20cm FDA UDI
Model / Reference
500118200M FDA UDI
Description
Echker & Ziegler Prostate Stabilization Set 18ga x 20cm FDA UDI

Identifiers

Catalog Number
1306 FDA UDI
Primary DI / UDI-DI
00886333225965 FDA UDI
FDA Product Code
IWJ FDA UDI
GMDN Term
Prostate brachytherapy system applicator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.5650 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

Category: Prostate brachytherapy system applicator, manual

Prostate Stabilization Set by Argon Medical Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Prostate brachytherapy system applicator, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1465e3e3-a6fd-4c94-8eb7-1c0c11d0f0a4 36 fields · synced Jun 9, 2026