Identity
- Trade Name
- Uline FDA UDI
- Generic Name
- Surgical/medical face mask, single-use FDA UDI
- Device Name
- Deluxe Surgical Mask FDA UDI
- Model / Reference
- S-22137 FDA UDI
- Description
- Deluxe Surgical Mask FDA UDI
Identifiers
- Catalog Number
- S-22137 FDA UDI
- Primary DI / UDI-DI
- 10851253007561 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical/medical face mask, single-use
Uline by Uline, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical/medical face mask, single-use.
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- 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
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
- Uline, Inc.
Sources (1)
- FDA UDI ce7dea7a-fa61-49f9-b005-0ca27de6bc59 34 fields · synced Jun 1, 2026