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Marina Medical 99-760

by Marina Medical Instruments, Inc.

Marina Medical 99-760 is a Class II device made by Marina Medical Instruments, Inc., listed in FDA GUDID since 18 Feb 2026 (UDI-DI 00840306837333), 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 Number00840306837333 UDI-DI Date18 Feb 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  • Withdrawn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
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
Model / Ref / Catalog
99-760
Primary DI / UDI-DI
00840306837333
FDA product code
GEI
GMDN term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 19.7 Centimeter

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Properties

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