Peribulbar Needle - Atkinson

FDA UDI

Class I (US FDA UDI)

by Hurricane Medical

Identity

Trade Name: Peribulbar Needle - Atkinson FDA UDI
Generic Name: Hypodermic needle, single-use FDA UDI
Device Name: Administering local anesthetic prior to ophthalmic surgery. FDA UDI
Model / Reference: 1425 FDA UDI
Description: Administering local anesthetic prior to ophthalmic surgery. FDA UDI

Identifiers

Catalog Number: 1425 FDA UDI
Primary DI / UDI-DI: 00813465010121 FDA UDI
FDA Product Code: GAA FDA UDI
GMDN Term: Hypodermic needle, 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 22 Millimeter FDA UDI
Needle Gauge — 25 Gauge FDA UDI

Category: Hypodermic needle, single-use

Peribulbar Needle - Atkinson by Hurricane Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hypodermic needle, single-use.

Monoject — Cardinalhealth · Class II
Pinpoint GT — Bard Access Systems, Inc. · Class II
Safety Needle — Jiangsu Micsafe Medical Technology Co., Ltd · Class IIa
Syringe w/Needle, Non-Toxic, 25G x 1", Luer Lock — Dynarex Corp. · Class II
Yeso med — WUXI YUSHOU MEDICAL APPLIANCES CO., LTD. · Class II
EasyTouch — MHC Medical Products · Class II
STERiJECT TM — TSK LABORATORY, JAPAN · Class II
Comfort EZ Pro — S.D.I. USA, INC. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Hurricane Medical

Sources (1)

FDA UDI 18aa01a6-b22d-4d6d-ba1c-6a34556d89d3 35 fields · synced Jun 1, 2026