Cranial Drill Bit, 5 pack

FDA UDI

Class II (US FDA UDI)

by Mazor Robotics Ltd

Identity

Trade Name: Cranial Drill Bit,5 pack FDA UDI
Generic Name: Muscle biopsy clamp FDA UDI
Device Name: Cranial Drill Bit,5 pack FDA UDI
Model / Reference: KIT0722-01 FDA UDI
Description: Cranial Drill Bit,5 pack FDA UDI

Identifiers

Primary DI / UDI-DI: 07290109180625 FDA UDI
FDA Product Code: HAW FDA UDI
LLZ FDA UDI
GMDN Term: Muscle biopsy clamp 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

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Muscle biopsy clamp

Cranial Drill Bit, 5 pack by Mazor Robotics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 e8be0b3a-e32f-47ad-a09a-8b910aa2a509 33 fields · synced Jun 1, 2026