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Cannulaide

FDA UDI

Class I (US FDA UDI)

by Salter Labs

Identity

Trade Name
Cannulaide FDA UDI
Generic Name
Universal patient tubing holder, non-sterile FDA UDI
Device Name
High Flow Cannulaide clear silicone cannula securement device for infants <1250 g FDA UDI
Model / Reference
HF101-0-25 FDA UDI
Description
High Flow Cannulaide clear silicone cannula securement device for infants <1250 g FDA UDI

Identifiers

Catalog Number
HF101-0-25 FDA UDI
Primary DI / UDI-DI
10607411007276 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Universal patient tubing holder, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5340 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Universal patient tubing holder, non-sterile

Cannulaide by Salter Labs — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Universal patient tubing holder, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Salter Labs

Sources (1)

  • FDA UDI 8359ddbd-c6e0-4d31-a5fb-8a215af76d1f 36 fields · synced May 30, 2026