Identity
- Trade Name
- Clear Choice FDA UDI
- Generic Name
- Face splash shield, single-use FDA UDI
- Device Name
- Frames FDA UDI
- Model / Reference
- SMI9211B FDA UDI
- Description
- Frames FDA UDI
Identifiers
- Catalog Number
- SMI9211B FDA UDI
- Primary DI / UDI-DI
- 10620974002854 FDA UDI
- FDA Product Code
- HOY FDA UDI
- GMDN Term
- Face splash shield, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4750 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
Yes
FDA UDI
Category: Face splash shield, single-use
Clear Choice by Southmedic Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Face splash shield, single-use.
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- Splash Shield — BERKLEY MEDICAL RESOURCES, INC. · Class II
- Crosstex™ — HU-FRIEDY MFG CO., LLC · Class I
- Splash Shield Lite — BERKLEY MEDICAL RESOURCES, INC. · Class II
- MedSource Face Shield — MEDSOURCE INTERNATIONAL LLC · Class I
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
- Southmedic Incorporated
Sources (1)
- FDA UDI 1c4ea946-83ce-4a42-8d71-817c0111f044 35 fields · synced May 30, 2026