Identity
- Trade Name
- MEDLINE FDA UDI
- Generic Name
- Peripheral intravenous catheterization support kit FDA UDI
- Device Name
- MIDLINE 5F DL FULL FDA UDI
- Model / Reference
- MIDST0023 FDA UDI
- Description
- MIDLINE 5F DL FULL FDA UDI
Identifiers
- Catalog Number
- MIDST0023 FDA UDI
- Primary DI / UDI-DI
- 10653160350590 FDA UDI
- FDA Product Code
- LRS FDA UDI
- GMDN Term
- Peripheral intravenous catheterization support kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5200 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
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
Yes
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
Category: Peripheral intravenous catheterization support kit
Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- IV Start Kit w/Catheter, 18Ga — Altitude Technologies Inc. · Class II
- Motion Medical Distributing — Haslam Medical, Inc. · Class II
- Centurion — Centurion Medical Products · Class II
- Curaplex — BOUND TREE MEDICAL, 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
- Medline Industries, Inc.
Sources (1)
- FDA UDI fb34044b-fc9c-4fc4-9e29-9b66210fad54 35 fields · synced Jun 8, 2026