Gass Retinal Detachment Hook

FDA UDI

Class I (US FDA UDI)

by Aurora Surgical, Llc

Identity

Trade Name: Gass Retinal Detachment Hook FDA UDI
Generic Name: Eye muscle hook, reusable FDA UDI
Device Name: Gass Retinal Detachment Hook FDA UDI
Model / Reference: AS8-061 FDA UDI
Description: Gass Retinal Detachment Hook FDA UDI

Identifiers

Catalog Number: AS8-061 FDA UDI
Primary DI / UDI-DI: 08175700134583 FDA UDI
FDA Product Code: HNQ FDA UDI
GMDN Term: Eye muscle hook, 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

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: Eye muscle hook, reusable

Gass Retinal Detachment Hook by Aurora 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: Aurora Surgical, Llc

Sources (1)

FDA UDI abce07fc-9942-4c19-8367-baaf894eda24 34 fields · synced Jun 6, 2026