Identity
- Trade Name
- Christmas Tree Connector - Non-Swivel FDA UDI
- Generic Name
- Nitrous oxide/oxygen quick-connect coupling, female FDA UDI
- Device Name
- Christmas Tree Connector - Non-Swivel (1/pack) FDA UDI
- Model / Reference
- RES001-1 FDA UDI
- Description
- Christmas Tree Connector - Non-Swivel (1/pack) FDA UDI
Identifiers
- Catalog Number
- RES001-1 FDA UDI
- Primary DI / UDI-DI
- 00848530060015 FDA UDI
- FDA Product Code
- BYX FDA UDI
- GMDN Term
- Nitrous oxide/oxygen quick-connect coupling, female FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5860 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Category: Nitrous oxide/oxygen quick-connect coupling, female
Christmas Tree Connector - Non-Swivel by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nitrous oxide/oxygen quick-connect coupling, female.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- SUNSET HEALTHCARE SOLUTIONS, Inc.
Sources (1)
- FDA UDI 514a9f5f-ec2e-4d28-89ec-81080578fdab 35 fields · synced May 31, 2026