Bone Pad Remover, Reusable

FDA UDI

Class I (US FDA UDI)

by Acra-Cut Inc

Identity

Trade Name: Bone Pad Remover, Reusable FDA UDI
Generic Name: Neurosurgical probe FDA UDI
Device Name: Left Hand Bone Pad Remover, Reusable FDA UDI
Model / Reference: 800-020L FDA UDI
Description: Left Hand Bone Pad Remover, Reusable FDA UDI

Identifiers

Catalog Number: 800-020L FDA UDI
Primary DI / UDI-DI: 00810607000507 FDA UDI
FDA Product Code: HAO FDA UDI
GMDN Term: Neurosurgical probe FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.4535 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

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical probe

Bone Pad Remover, Reusable by Acra-Cut Inc — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Acra-Cut Inc

Sources (1)

FDA UDI 0f6b5749-b56f-458b-a620-6d125e4d2bde 35 fields · synced May 30, 2026