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Marina Medical 270-003

by Marina Medical Instruments, Inc.

Marina Medical 270-003 is a Class I device made by Marina Medical Instruments, Inc., listed in FDA GUDID since 9 May 2024 (UDI-DI 00840306826573), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840306826573 UDI-DI Date9 May 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Marina Medical
Generic name
Vaginal dilator
Model / Ref / Catalog
270-003
Primary DI / UDI-DI
00840306826573
FDA product code
HDQ
GMDN term
Vaginal dilator
Device class
Class I
Regulation number
884.4530
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Width — 2.54 Centimeter

Related devices

Category: Vaginal dilator

Other devices from Marina Medical Instruments, Inc.

See all devices from Marina Medical Instruments, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)