Identity
- Trade Name
- Argyle FDA UDI
- Generic Name
- Non-ISO80369-standardized small-bore multichannel connector, single-use FDA UDI
- Device Name
- Argyle™ Y Connector, Polypropylene, Large FDA UDI
- Model / Reference
- 8888272005 FDA UDI
- Description
- Argyle™ Y Connector, Polypropylene, Large FDA UDI
Identifiers
- Catalog Number
- 8888272005 FDA UDI
- Primary DI / UDI-DI
- 50192253018569 FDA UDI
- FDA Product Code
- BYY FDA UDI
- GMDN Term
- Non-ISO80369-standardized small-bore multichannel connector, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Non-ISO80369-standardized small-bore multichannel connector, single-use
Argyle by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Non-ISO80369-standardized small-bore multichannel connector, single-use.
- CONNECTOR, Y 1/4" X 1/4" X 1/4" W/OUT LUER — NOVOSCI CORP. · Class I
- CONNECTOR, Y 3/8" X 1/4" X 3/8" — NOVOSCI CORP. · Class II
- CONNECTOR, Y 3/8" X 3/8" X 1/2" W/OUT LUER — NOVOSCI CORP. · Class I
- CONNECTOR, 3/8" X 3/8" X 1/4" CLEAR PAY — NOVOSCI CORP. · Class II
- CONNECTOR, EQUAL Y 1/2" — NOVOSCI CORP. · Class II
- CONNECTOR, 1/4" X 1/4" X 3/8" CLEAR PAY — NOVOSCI CORP. · Class II
- CONNECTOR, Y 1/2" X 1/2" X 3/8" — NOVOSCI CORP. · Class II
- CONNECTOR, Y 1/2" X 1/2" X 1/2" W/OUT LUER — NOVOSCI CORP. · Class I
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
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 56c8c686-cb5f-4d98-9b97-70561f640ea4 34 fields · synced Jun 8, 2026