Goio

FDA UDI

Class I (US FDA UDI)

by WaisMed Ltd

Identity

Trade Name: GOIO FDA UDI
Generic Name: Intravenous line stopcock FDA UDI
Device Name: Intraosseous start kit by PerSys Medical FDA UDI
Model / Reference: GOIO without Fixation FDA UDI
Description: Intraosseous start kit by PerSys Medical FDA UDI

Identifiers

Primary DI / UDI-DI: 17290008325100 FDA UDI
FDA Product Code: GAX FDA UDI
OJA FDA UDI
FPA FDA UDI
GMDN Term: Intravenous line stopcock FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.5900 FDA UDI
880.5440 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

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

Category: Intravenous line stopcock

Goio by WaisMed Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous line stopcock.

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Kabi Access Infusion Sets — CODAN US Corporation · Class II
SPC-4(4-WAY STOPCOCK) — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
CLEARLINK/CONTINU-FLO — BAXTER INTERNATIONAL INC. · Class II
ICU Medical — ICU MEDICAL, INC. · Class II
ICU Medical — ICU MEDICAL, INC. · Class II
VYGON — Vygon Corp. · 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

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Manufacturer

Manufacturer: WaisMed Ltd

Sources (1)

FDA UDI 9fc83012-9b30-42a8-8d59-87cb7c59cb2d 33 fields · synced May 30, 2026