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Msi NHLRS3

by Modern Surgical Instruments LLC

Msi NHLRS3 is a Class I device made by Modern Surgical Instruments LLC, listed in FDA GUDID since 15 Oct 2026 (UDI-DI 00810130207589), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810130207589 UDI-DI Date15 Oct 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  • Withdrawn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
Msi
Generic name
Surgical retractor/retraction system blade, reusable
Model / reference
NHLRS3
Primary DI / UDI-DI
00810130207589
FDA product code
GAD
GMDN term
Surgical retractor/retraction system blade, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Modern Surgical Instruments LLC

See all devices from Modern Surgical Instruments LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)