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2-Can™

FDA UDI

Class I (US FDA UDI)

by Flow-Fx, LLC

Identity

Trade Name
2-CAN™ FDA UDI
Generic Name
Orthopaedic coaxial injection applicator FDA UDI
Device Name
2-CAN™ 450mm Delivery Cannula FDA UDI
Model / Reference
2CAN450B FDA UDI
Description
2-CAN™ 450mm Delivery Cannula FDA UDI

Identifiers

Catalog Number
2CAN450B FDA UDI
Primary DI / UDI-DI
B2672CAN450B0 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Orthopaedic coaxial injection applicator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 450 Millimeter FDA UDI
Outer Diameter — 7.8 Millimeter FDA UDI

Category: Orthopaedic coaxial injection applicator

2-Can™ by Flow-Fx, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic coaxial injection applicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flow-Fx, LLC

Sources (1)

  • FDA UDI 923dc24d-81a3-4b95-b5e5-b4b6fc531666 36 fields · synced May 29, 2026