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Philips

FDA UDI

Class I (US FDA UDI)

by Philips Medical Systems Nederland B.V.

Identity

Trade Name
Philips FDA UDI
Generic Name
Needle guide, single-use FDA UDI
Device Name
Kit, Enhanced Access, Bilateral Upgrade consists of Fiducial Marker Grid Block Assembly; 3 Grid Plate Enhanced Access, Lateral; 3 Grid Plate, Enhanced Access Medial; 2 IMMOBILIZATION SYSTEM, M/L, LBS ENHANCED; MRI Needle Block 12G; MRI Needle Block 14G; MRI Needle Block 18G; 2 Needle Block Holder; MRI Needle Block 16G. FDA UDI
Model / Reference
989603207293 FDA UDI
Description
Kit, Enhanced Access, Bilateral Upgrade consists of Fiducial Marker Grid Block Assembly; 3 Grid Plate Enhanced Access, Lateral; 3 Grid Plate, Enhanced Access Medial; 2 IMMOBILIZATION SYSTEM, M/L, LBS ENHANCED; MRI Needle Block 12G; MRI Needle Block 14G; MRI Needle Block 18G; 2 Needle Block Holder; MRI Needle Block 16G. FDA UDI

Identifiers

Primary DI / UDI-DI
00884838118775 FDA UDI
FDA Product Code
PXP FDA UDI
GMDN Term
Needle guide, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Needle guide, single-useNeedle guide, reusable

Philips by Philips Medical Systems Nederland B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 069645ba-5261-46ef-8e66-a480d1c1b692 35 fields · synced Sep 18, 2026