Identity
- Trade Name
- AVANOS FDA UDI
- Generic Name
- Suction system catheter, general-purpose FDA UDI
- Device Name
- Replacement Catheter for Neonates / Pediatrics FDA UDI
- Model / Reference
- B50811 FDA UDI
- Description
- Replacement Catheter for Neonates / Pediatrics FDA UDI
Identifiers
- Catalog Number
- B50811 FDA UDI
- Primary DI / UDI-DI
- 00609038000237 FDA UDI
- FDA Product Code
- BSY FDA UDI
- GMDN Term
- Suction system catheter, general-purpose FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.6810 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Yes
FDA UDI
MR Conditional FDA UDI
Avanos by Avanos Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Avanos Medical, Inc.
Sources (1)
- FDA UDI 3e1dc678-1fd7-4f0f-90d6-297f2889fcba 36 fields · synced Jun 9, 2026