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Rear Panel Adaptor

FDA UDI

Class II (US FDA UDI)

by Mazor Robotics Ltd

Identity

Trade Name
Rear Panel Adaptor FDA UDI
Generic Name
Stereotactic surgery system probe, reusable FDA UDI
Model / Reference
MAS1891-06S FDA UDI

Identifiers

Primary DI / UDI-DI
07290115751581 FDA UDI
510(k) Number
K203005 FDA UDI
FDA Product Code
OLO 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Stereotactic surgery system probe, reusable

Rear Panel Adaptor by Mazor Robotics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stereotactic surgery system probe, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mazor Robotics Ltd

Sources (1)

  • FDA UDI 93ea4a89-9d1f-46ff-a30f-fdf391aae78d 33 fields · synced Jun 8, 2026