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Sun Nuclear MICRO MLG 150

by Sun Nuclear Corporation

Sun Nuclear MICRO MLG 150 (805708) is a Class I device made by Sun Nuclear Corporation, listed in FDA GUDID since 25 Jan 2021 (UDI-DI B136MLG1500), 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 NumberB136MLG1500 UDI-DI Date25 Jan 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sun Nuclear MICRO
Generic name
Laser patient positioning system
Model / Ref / Catalog
MLG 150, 805708
Primary DI / UDI-DI
B136MLG1500
FDA product code
IWE
GMDN term
Laser patient positioning system
Device class
Class I
Regulation number
892.5780
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

From the manufacturer

Manufacturer's product page: Sun Nuclear Patents

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)