Identity
- Trade Name
- SHIELDMATE FDA UDI
- Generic Name
- Eye splash shield, single-use FDA UDI
- Device Name
- TIE FACEMASK, W/SHIELD & MAGIC ARCH, ANTIFOG STRIP, BLUE BULK PACK 100 FDA UDI
- Model / Reference
- SHI BL 8101 SB FDA UDI
- Description
- TIE FACEMASK, W/SHIELD & MAGIC ARCH, ANTIFOG STRIP, BLUE BULK PACK 100 FDA UDI
Identifiers
- Catalog Number
- SHI BL 8101 SB FDA UDI
- Primary DI / UDI-DI
- 00817583020543 FDA UDI
- 510(k) Number
- K882027 FDA UDI
- FDA Product Code
- FXX FDA UDI
- GMDN Term
- Eye splash shield, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4040 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
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Eye splash shield, single-use
Shieldmate by Alphaprotech, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K882027 also covers:
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 II | Pending data |
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Manufacturer
- Manufacturer
- Alphaprotech, Inc.
Sources (1)
- FDA UDI 9bcc806b-f850-42e6-9b98-88e3e01b93cf 36 fields · synced May 30, 2026