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Invivo

FDA UDI

Class II (US FDA UDI)

by Philips DS North America LLC

Identity

Trade Name
Invivo FDA UDI
Generic Name
MRI system coil, radio-frequency FDA UDI
Device Name
Kit, Enhanced Access, Bilateral Upgrade consists of Fiducial Marker Block; 3 Grid Plates Enhanced Access-Lateral; 3 Grid Plates Enhanced Access-Medial; 2 Immobilization system Enhanced-M/L; MRI Needle Block 12G for; MRI Needle Block 14G; MRI Needle Block 18G; 2 MRI Needle Block 12G; MRI Needle Block 16G. FDA UDI
Model / Reference
9896-032-07292 FDA UDI
Description
Kit, Enhanced Access, Bilateral Upgrade consists of Fiducial Marker Block; 3 Grid Plates Enhanced Access-Lateral; 3 Grid Plates Enhanced Access-Medial; 2 Immobilization system Enhanced-M/L; MRI Needle Block 12G for; MRI Needle Block 14G; MRI Needle Block 18G; 2 MRI Needle Block 12G; MRI Needle Block 16G. FDA UDI

Identifiers

Primary DI / UDI-DI
00884838115279 FDA UDI
FDA Product Code
MOS FDA UDI
GMDN Term
MRI system coil, radio-frequency FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1000 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: MRI system coil, radio-frequency

Invivo by Philips DS North America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as MRI system coil, radio-frequency.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6787c67f-347e-4f3b-adbb-e2523edbf32d 34 fields · synced Jun 8, 2026