Surgipros

FDA UDI

Class I (US FDA UDI)

by Surgipros Llc

Identity

Trade Name: SURGIPROS FDA UDI
Generic Name: Neurosurgical curette, single-use FDA UDI
Device Name: 2-0 MICRO CERVICAL CURETTE ANGLED 10" RED FDA UDI
Model / Reference: 875-384SP FDA UDI
Description: 2-0 MICRO CERVICAL CURETTE ANGLED 10" RED FDA UDI

Identifiers

Primary DI / UDI-DI: 00810143901368 FDA UDI
FDA Product Code: FZS FDA UDI
GMDN Term: Neurosurgical curette, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical curette, single-use

Surgipros by Surgipros 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: Surgipros Llc

Sources (1)

FDA UDI 0cef0db0-3027-45e1-8efa-a381f8aee224 34 fields · synced Jun 1, 2026