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SolidAIRity Flex

FDA UDI

Class I (US FDA UDI)

by Securisyn Medical, Llc

Identity

Trade Name
SolidAIRity Flex FDA UDI
Generic Name
Endotracheal tube holder FDA UDI
Device Name
Oral Endotracheal Tube Stabilizer, Replacement Neck Straps FDA UDI
Model / Reference
4.1500.3 FDA UDI
Description
Oral Endotracheal Tube Stabilizer, Replacement Neck Straps FDA UDI

Identifiers

Catalog Number
4.1500.3 FDA UDI
Primary DI / UDI-DI
10860009077918 FDA UDI
FDA Product Code
CBH FDA UDI
GMDN Term
Endotracheal tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5770 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endotracheal tube holder

SolidAIRity Flex by Securisyn Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endotracheal tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ec63431-a14f-4b9c-9e1b-a0a70a6c18f7 34 fields · synced May 30, 2026