Ingenia, MR 5300, MR 7700, Achieva 782161

GUDID 00884838115729

Upgrades dStream to R12

Philips Medical Systems Nederland B.V.

Full-body MRI system, superconducting magnet

• Primary Device ID: 00884838115729
• NIH Device Record Key: f8445add-0485-49e4-9f22-95d70d078786
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ingenia, MR 5300, MR 7700, Achieva
• Version Model Number: Upgrades dStream to R12
• Catalog Number: 782161
• Company DUNS: 413819707
• Company Name: Philips Medical Systems Nederland B.V.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838115729 [Primary]

FDA Product Code

• LNH: System, Nuclear Magnetic Resonance Imaging

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-12-15
• Device Publish Date: 2025-10-06

Devices Manufactured by Philips Medical Systems Nederland B.V.

• 00884838128415 - Ingenia: 2026-01-15 BlueSeal SE
• 00884838128422 - Ingenia: 2026-01-15 BlueSeal XE
• 00884838128439 - Ingenia: 2026-01-15 MR 7700
• 00884838128446 - Ingenia: 2026-01-15 MR 5300
• 00884838128453 - Ingenia: 2026-01-15 Ingenia Elition S
• 00884838128460 - Ingenia: 2026-01-15 Ingenia Elition X
• 00884838128477 - Ingenia, MR5300, MR7700, Achieva: 2026-01-15 Ingenia Ambition S
• 00884838128484 - Ingenia 3.0T: 2026-01-15 Ingenia Ambition X