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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 speculum, reusable FDA UDI
Device Name
. Jackson Speculum - Medium: Size: 8.9cm x 3.8cm/3.5in x 1.5in with Non-Conductive Coating/DSE CLIP FDA UDI
Model / Reference
254-735NC FDA UDI
Description
. Jackson Speculum - Medium: Size: 8.9cm x 3.8cm/3.5in x 1.5in with Non-Conductive Coating/DSE CLIP FDA UDI

Identifiers

Catalog Number
254-735NC FDA UDI
Primary DI / UDI-DI
00840306825736 FDA UDI
FDA Product Code
HDF FDA UDI
GMDN Term
Vaginal speculum, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4520 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
Length — 8.9 Centimeter FDA UDI

Category: Vaginal speculum, reusable

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 speculum, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ebe4ca4f-db1b-4df1-a397-79321fade1b3 36 fields · synced May 30, 2026