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Marina Medical

FDA UDI

Class I (US FDA UDI)

by Marina Medical Instruments, Inc.

Identity

Trade Name
Marina Medical FDA UDI
Generic Name
Vaginal dilator FDA UDI
Device Name
VVD Veronikis Vaginal Dilator, 3cm Tip, 2.54cm Width FDA UDI
Model / Reference
270-003 FDA UDI
Description
VVD Veronikis Vaginal Dilator, 3cm Tip, 2.54cm Width FDA UDI

Identifiers

Catalog Number
270-003 FDA UDI
Primary DI / UDI-DI
00840306826573 FDA UDI
FDA Product Code
HDQ FDA UDI
GMDN Term
Vaginal dilator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 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

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
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 2.54 Centimeter FDA UDI

Category: Vaginal dilator

Marina Medical by Marina Medical Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal dilator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6113dd3b-8290-4210-8e90-872d81d17839 36 fields · synced May 31, 2026