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063377717

FDA UDI

Class II (US FDA UDI)

by Philips Ultrasound LLC

Identity

Trade Name
063377717 FDA UDI
Generic Name
Multi-purpose stereotactic surgery system FDA UDI
Model / Reference
063377717 FDA UDI

Identifiers

Primary DI / UDI-DI
00884838081239 FDA UDI
FDA Product Code
IYO FDA UDI
LLZ FDA UDI
JAK FDA UDI
GMDN Term
Multi-purpose stereotactic surgery system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
892.2050 FDA UDI
892.1750 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-purpose stereotactic surgery system

063377717 by Philips Ultrasound LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose stereotactic surgery system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9dad5247-4892-4e59-8db2-2cb5537989db 32 fields · synced Jun 8, 2026