Goio

FDA UDI

Class I (US FDA UDI)

by WaisMed Ltd

Identity

Trade Name: GOIO FDA UDI
Generic Name: First aid absorbent pad/bandage FDA UDI
Device Name: Intraosseous start kit by PerSys Medical FDA UDI
Model / Reference: GOIO FDA UDI
Description: Intraosseous start kit by PerSys Medical FDA UDI

Identifiers

Primary DI / UDI-DI: 17290008325018 FDA UDI
FDA Product Code: KMK FDA UDI
GAX FDA UDI
OJA FDA UDI
FPA FDA UDI
GMDN Term: First aid absorbent pad/bandage FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5210 FDA UDI
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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: First aid absorbent pad/bandage Intravenous line stopcock

Goio by WaisMed Ltd — 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: WaisMed Ltd

Sources (1)

FDA UDI 94a5a7db-f176-4199-a627-97b02e046162 33 fields · synced May 30, 2026