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GO IO Intraosseous Start Kit 12/Case

FDA UDI

Class II (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
GO IO Intraosseous Start Kit 12/Case FDA UDI
Generic Name
Intravenous line stopcock FDA UDI
Device Name
Secure IV and NIO Fixation FDA UDI
Model / Reference
03 FDA UDI
Description
Secure IV and NIO Fixation FDA UDI

Identifiers

Catalog Number
GO IO FDA UDI
Primary DI / UDI-DI
M689GOIO030 FDA UDI
FDA Product Code
OJA FDA UDI
GMDN Term
Intravenous line stopcock FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravenous line stopcock

GO IO Intraosseous Start Kit 12/Case by Safeguard Us Operating, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous line stopcock.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4a0a5cc7-592a-45f0-aebd-44fcf21715ef 36 fields · synced Jun 8, 2026