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Marina Medical 200-281

by Marina Medical Instruments, Inc.

Marina Medical 200-281 is a Class I device made by Marina Medical Instruments, Inc., listed in FDA GUDID since 11 May 2026 (UDI-DI 00840306837388), 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 Number00840306837388 UDI-DI Date11 May 2026ListedStatusListed 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  • Withdrawn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
Plastic surgery osteotome
Model / Ref / Catalog
200-281
Primary DI / UDI-DI
00840306837388
FDA product code
GFI
GMDN term
Plastic surgery osteotome
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 6 Millimeter

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)