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Vaginal Applicator, 20mm

FDA UDI

Class II (US FDA UDI)

by Icad, Inc.

Identity

Trade Name
Vaginal Applicator, 20mm FDA UDI
Generic Name
Intraoperative/postoperative therapeutic x-ray system vaginal applicator FDA UDI
Device Name
Vaginal Applicator 20 mm FDA UDI
Model / Reference
720267 FDA UDI
Description
Vaginal Applicator 20 mm FDA UDI

Identifiers

Catalog Number
AG3020 FDA UDI
Primary DI / UDI-DI
00858012005472 FDA UDI
510(k) Number
K072616 FDA UDI
FDA Product Code
JAD FDA UDI
GMDN Term
Intraoperative/postoperative therapeutic x-ray system vaginal applicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5900 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Intraoperative/postoperative therapeutic x-ray system vaginal applicator

Vaginal Applicator, 20mm by Icad, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraoperative/postoperative therapeutic x-ray system vaginal applicator.

Cleared under the same submission

K072616 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icad, Inc.

Sources (1)

  • FDA UDI 0307a4ae-1d85-46cd-aa08-819f529ee311 35 fields · synced Jun 1, 2026