Identity
- Trade Name
- Argyle FDA UDI
- Generic Name
- Arm procedure positioner, reusable FDA UDI
- Device Name
- Argyle I.V. Support Board FDA UDI
- Model / Reference
- MI00850 FDA UDI
- Description
- Argyle I.V. Support Board FDA UDI
Identifiers
- Catalog Number
- MI00850- FDA UDI
- Primary DI / UDI-DI
- 10192253021127 FDA UDI
- FDA Product Code
- BTX FDA UDI
- GMDN Term
- Arm procedure positioner, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.3910 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
No
FDA UDI
Over-the-Counter
Yes
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
Dimensions & Sizes
- Size
- Width — 4.8 Centimeter FDA UDILength — 12.4 Centimeter FDA UDI
Category: Arm procedure positioner, reusable
Argyle by Cardinal Health 200, 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
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI e748c0da-4a9f-480e-a1b8-c0bcec9e83d5 35 fields · synced Jun 8, 2026