Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name: Ambler Surgical FDA UDI
Generic Name: Intraocular scissors probe-tip, reusable FDA UDI
Device Name: Ambler MICS scissors tip, 2'', 20 gauge, 360 degrees rotatable, working length 30mm, curved with falcated 2.0mm long blades, titanium For use with MICS handle #9910T FDA UDI
Model / Reference: Ambler MICS scissors tip FDA UDI
Description: Ambler MICS scissors tip, 2'', 20 gauge, 360 degrees rotatable, working length 30mm, curved with falcated 2.0mm long blades, titanium For use with MICS handle #9910T FDA UDI

Identifiers

Catalog Number: 9924T FDA UDI
Primary DI / UDI-DI: 00190660156558 FDA UDI
FDA Product Code: HNF FDA UDI
GMDN Term: Intraocular scissors probe-tip, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 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: Intraocular scissors probe-tip, reusable

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 5e58e633-f7f9-45af-bec8-8dcdb12607bc 35 fields · synced May 30, 2026