Low Profile Cervical Curette

FDA UDI

Class I (US FDA UDI)

by Neuroenterprises Llc

Identity

Trade Name: Low Profile Cervical Curette FDA UDI
Generic Name: Neurosurgical curette, single-use FDA UDI
Device Name: Cervical spinal stenosis curette FDA UDI
Model / Reference: NE5 FDA UDI
Description: Cervical spinal stenosis curette FDA UDI

Identifiers

Primary DI / UDI-DI: 00860006017736 FDA UDI
FDA Product Code: HAO FDA UDI
GMDN Term: Neurosurgical curette, single-use 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

Yes

FDA UDI

Single Use

Yes

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 curette, single-use

Low Profile Cervical Curette by Neuroenterprises Llc — 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: Neuroenterprises Llc

Sources (1)

FDA UDI c0b0a623-ff35-4f14-880b-5a843557c8fa 33 fields · synced May 30, 2026