Identity
- Trade Name
- Argyle FDA UDI
- Generic Name
- Gastric lavage system FDA UDI
- Device Name
- True content to be populated as part of rebranding FDA UDI
- Model / Reference
- 8888750513 FDA UDI
- Description
- True content to be populated as part of rebranding FDA UDI
Identifiers
- Catalog Number
- 8888750513 FDA UDI
- Primary DI / UDI-DI
- 10192253013023 FDA UDI
- FDA Product Code
- KDH FDA UDI
- GMDN Term
- Gastric lavage 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Gastric lavage system
Argyle by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Gastric lavage system.
- Argyle — Cardinalhealth · Class II
- Relish — Shenzhen Relish Technology Co., Ltd · Class II
- Argyle — Cardinalhealth · Class II
- Argyle — Cardinal Health 200, LLC · 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
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI cf61000c-5b72-4694-95f2-70b6cf6492ca 34 fields · synced Jun 8, 2026