Identity
- Trade Name
- SAM IO Intraosseous Access System FDA UDI
- Generic Name
- Catheter/tubing connection protector FDA UDI
- Device Name
- SAM IO Stabilizer - 5 Pack FDA UDI
- Model / Reference
- IO740-5P-EN FDA UDI
- Description
- SAM IO Stabilizer - 5 Pack FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10822045000305 FDA UDI
- FDA Product Code
- KMK FDA UDI
- GMDN Term
- Catheter/tubing connection protector FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5210 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
Category: Catheter/tubing connection protector
SAM IO Intraosseous Access System by SAM Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Catheter/tubing connection protector.
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
- SAM Medical Products
Sources (1)
- FDA UDI e346251f-c052-4dcc-9eaa-fb05b2004629 34 fields · synced Jun 8, 2026