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Surgivisio Device

FDA UDI

Class II (US FDA UDI)

by Ecential Robotics

Identity

Trade Name
SURGIVISIO DEVICE FDA UDI
Generic Name
Mobile general-purpose fluoroscopic x-ray system, digital FDA UDI
Model / Reference
I01001 FDA UDI

Identifiers

Primary DI / UDI-DI
03701311501121 FDA UDI
FDA Product Code
OLO FDA UDI
OWB FDA UDI
JAA FDA UDI
OXO FDA UDI
GMDN Term
Mobile general-purpose fluoroscopic x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
892.1650 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

Yes

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

Yes

FDA UDI

Category: Robotic surgical navigation systemOptical surgical navigation device tracking systemMobile general-purpose fluoroscopic x-ray system, digital

Surgivisio Device by Ecential Robotics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile general-purpose fluoroscopic x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ecential Robotics

Sources (1)

  • FDA UDI 694b5e0d-d78d-4267-9a3f-70088fc260d7 33 fields · synced Jun 1, 2026