Identity
- Trade Name
- Beesure FDA UDI
- Generic Name
- Neurofibromatosis type 1 IVD, control FDA UDI
- Device Name
- Beesure Level 2 Face Mask 50 /BX , White FDA UDI
- Model / Reference
- BE2100W FDA UDI
- Description
- Beesure Level 2 Face Mask 50 /BX , White FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10817508020358 FDA UDI
- FDA Product Code
- LYU FDA UDI
- GMDN Term
- Neurofibromatosis type 1 IVD, control FDA UDI
Classification
- Device Class
- Class I 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
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: Neurofibromatosis type 1 IVD, control
Beesure by Ascend Eagle Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Neurofibromatosis type 1 IVD, control.
- Beesure — ASCEND EAGLE INCORPORATED · Class I
- Beesure — ASCEND EAGLE INCORPORATED · Class I
- Beesure — ASCEND EAGLE INCORPORATED · Class I
- Beesure — ASCEND EAGLE INCORPORATED · Class I
- Beesure — ASCEND EAGLE INCORPORATED · 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
- Ascend Eagle Incorporated
Sources (1)
- FDA UDI d131ab8e-50ef-4c52-8aec-2904a77058b5 34 fields · synced Jun 1, 2026