Surgical_instruments, Bed Connector

FDA UDI

Class II (US FDA UDI)

by Mazor Robotics Ltd

Identity

Trade Name: SURGICAL_INSTRUMENTS, BED CONNECTOR FDA UDI
Generic Name: Stereotactic surgery system probe, reusable FDA UDI
Model / Reference: TOL0085-01 FDA UDI

Identifiers

Primary DI / UDI-DI: 07290109183732 FDA UDI
FDA Product Code: HAW FDA UDI
LLZ FDA UDI
GMDN Term: Stereotactic surgery system probe, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4560 FDA UDI
892.2050 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Stereotactic surgery system probe, reusable

Surgical_instruments, Bed Connector by Mazor Robotics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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ASTRA Spine System — SPINECRAFT LLC · Class II
Navigation — SPINEOLOGY INC. · Class II
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Mazor Robotics Ltd

Sources (1)

FDA UDI 58c007f8-e65f-47d6-b0f5-6b489d2d711c 33 fields · synced May 30, 2026