Identity
- Trade Name
- Argyle FDA UDI
- Generic Name
- Low-pressure tubing connector, reusable FDA UDI
- Device Name
- 5-in-1 Bubble Connector,Vinyl FDA UDI
- Model / Reference
- 8888271106 FDA UDI
- Description
- 5-in-1 Bubble Connector,Vinyl FDA UDI
Identifiers
- Catalog Number
- 8888271106 FDA UDI
- Primary DI / UDI-DI
- 10884521031654 FDA UDI
- FDA Product Code
- GAZ FDA UDI
- GMDN Term
- Low-pressure tubing connector, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
Argyle by Cardinalhealth — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cardinalhealth
Sources (1)
- FDA UDI 5035808f-4c6f-40a4-ae34-245846bb163e 38 fields · synced May 31, 2026