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Invivo dS Microscopy 47mm Coil, Ingenia 3.0T

by Philips Ds North America LLC

Invivo dS Microscopy 47mm Coil, Ingenia 3.0T (45353035833) is a Class II device made by Philips Ds North America LLC, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00884838065536), 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 Number00884838065536 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
Invivo
Generic name
MRI system coil, radio-frequency
Model / Ref / Catalog
dS Microscopy 47mm Coil, Ingenia 3.0T, 45353035833
Primary DI / UDI-DI
00884838065536
FDA product code
MOS
GMDN term
MRI system coil, radio-frequency
Device class
Class II
Regulation number
892.1000
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

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Properties

  • Serial number
Other properties (14, all answered No)