Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name: Ambler Surgical FDA UDI
Generic Name: Neurosurgical curette, single-use FDA UDI
Device Name: Lumbar axial curette, 10 1/4'', angled shaft, low profile, straight down, size #2/0 cup, square handle FDA UDI
Model / Reference: Lumbar axial curette FDA UDI
Description: Lumbar axial curette, 10 1/4'', angled shaft, low profile, straight down, size #2/0 cup, square handle FDA UDI

Identifiers

Catalog Number: 18-960 FDA UDI
Primary DI / UDI-DI: 00190660203047 FDA UDI
FDA Product Code: HTF 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

Yes

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

Yes

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

Ambler Surgical by Ambler Surgical, 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: Ambler Surgical, LLC

Sources (1)

FDA UDI 4daef4e2-cd87-47db-9365-a41917d8d2bb 35 fields · synced May 30, 2026