Identity
- Trade Name
- 2-CAN™ FDA UDI
- Generic Name
- Orthopaedic coaxial injection applicator FDA UDI
- Device Name
- 6.5mm 2-CAN (4.8mm Outer Diameter) FDA UDI
- Model / Reference
- 103-1-03 FDA UDI
- Description
- 6.5mm 2-CAN (4.8mm Outer Diameter) FDA UDI
Identifiers
- Catalog Number
- 103-1-03 FDA UDI
- Primary DI / UDI-DI
- B2671031030 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
- Outer Diameter — 4.8 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
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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
- Flow-Fx, LLC
Sources (1)
- FDA UDI 8d1697aa-504e-4eab-9b7e-6f3a44d153ae 35 fields · synced May 30, 2026