Identity
- Trade Name
- Argyle FDA UDI
- Generic Name
- Thoracic suction system FDA UDI
- Device Name
- Luki Tube Specimen Collection Device,20 mL FDA UDI
- Model / Reference
- 8886864604 FDA UDI
- Description
- Luki Tube Specimen Collection Device,20 mL FDA UDI
Identifiers
- Catalog Number
- 8886864604 FDA UDI
- Primary DI / UDI-DI
- 30884527000108 FDA UDI
- FDA Product Code
- KDH FDA UDI
- GMDN Term
- Thoracic suction system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5980 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
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 6.25 Inch FDA UDITotal Volume — 20 Milliliter FDA UDI
Category: Thoracic suction system
Argyle by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Thoracic suction system.
- OCEAN — Atrium Medical Corp. · Class II
- OASIS — Atrium Medical Corp. · Class II
- Argyle — Cardinalhealth · Class II
- Altitude — Cardinalhealth · Class II
- Argyle — Cardinalhealth · Class II
- Argyle — Cardinalhealth · Class II
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 |
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Manufacturer
- Manufacturer
- Cardinalhealth
Sources (1)
- FDA UDI 64ec46dc-86fc-4f50-b924-36003d396fcb 37 fields · synced Jun 1, 2026