Identity
- Trade Name
- Beesure FDA UDI
- Generic Name
- Sterilization packaging, single-use FDA UDI
- Device Name
- Beesure Sterilization Pouch 200 /BAG , 3 1/2" x 10 1/2" FDA UDI
- Model / Reference
- BE1231 FDA UDI
- Description
- Beesure Sterilization Pouch 200 /BAG , 3 1/2" x 10 1/2" FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10817508020020 FDA UDI
- FDA Product Code
- FRG FDA UDI
- GMDN Term
- Sterilization packaging, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 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: Sterilization packaging, single-use
Beesure by Ascend Eagle Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Ascend Eagle Incorporated
Sources (1)
- FDA UDI be344713-15a5-4235-b6c9-179df0ad7ba4 34 fields · synced Jun 1, 2026