Identity
- Trade Name
- Medline ReNewal FDA UDI
- Generic Name
- Medical gas/vacuum pipeline system FDA UDI
- Device Name
- MANIFOLD, DORNOCH, REPROCESSED FDA UDI
- Model / Reference
- ULCL500R FDA UDI
- Description
- MANIFOLD, DORNOCH, REPROCESSED FDA UDI
Identifiers
- Catalog Number
- ULCL500R FDA UDI
- Primary DI / UDI-DI
- 10888277188655 FDA UDI
- FDA Product Code
- GCY FDA UDI
- GMDN Term
- Medical gas/vacuum pipeline system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4680 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
Dimensions & Sizes
- Size
- Outer Diameter — 2.65 Inch FDA UDI
Category: Medical gas/vacuum pipeline system
Medline ReNewal by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Medical gas/vacuum pipeline system.
- Flotec — Flotec, Inc. · Class I
- Medline ReNewal — MEDLINE INDUSTRIES, INC. · Class II
- Medline ReNewal — MEDLINE INDUSTRIES, INC. · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Medline Industries, Inc.
Sources (1)
- FDA UDI f522f0db-af84-4f69-b477-14c19a268dea 36 fields · synced May 30, 2026