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BriteBlade Pro Evo Single-Use Fiber Optic Miller 00
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- BriteBlade Pro Evo Single-Use Fiber Optic Miller 00 FDA UDI
- Generic Name
- Laryngoscope blade, single-use FDA UDI
- Model / Reference
- 040-760NU FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055788773535 FDA UDI
- FDA Product Code
- CCW FDA UDI
- GMDN Term
- Laryngoscope blade, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Laryngoscope blade, single-use
A comprehensive medical device directory, including detailed information on the BriteBlade Pro Evo Single-Use Fiber Optic Miller 00. This device is a laryngoscope blade designed for safe and effective intubation.
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Flexicare Medical Limited
Sources (1)
- FDA UDI bc8ad63f-1acb-47df-8292-8f9b8e1573e2 32 fields · synced Jul 23, 2026