Identity
- Trade Name
- Ear-Friendly Mask FDA UDI
- Generic Name
- Surgical/medical face mask, single-use FDA UDI
- Model / Reference
- Ear-Friendly Mask FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800003025008 FDA UDI
- 510(k) Number
- K211105 FDA UDI
- FDA Product Code
- FXX FDA UDI
- GMDN Term
- Surgical/medical face mask, 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical/medical face mask, single-use
Ear-Friendly Mask by Ray Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical/medical face mask, single-use.
- ProGear — Prestige Ameritech · Class II
- Precept® — Precept Medical Products, Inc. · Class II
- hcs — DYAD MEDICAL SOURCING, LLC · Class I
- Precept® — Precept Medical Products, Inc. · Class II
- AOSHANG — Tianjin Aoshang Outdoor Equipment Co., Ltd. · Class II
- Precept® — Precept Medical Products, Inc. · Class II
- Precept® — Precept Medical Products, Inc. · Class II
- Surgical Face Mask — Foshan Nanhai Plus Medical Co., Ltd · Class II
Cleared under the same submission
K211105 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
- Ray Co., Ltd
Sources (1)
- FDA UDI 6a5b0110-e70c-454a-904f-a4950fcbab79 33 fields · synced May 30, 2026