Identity
- Trade Name
- Medline ReNewal FDA UDI
- Generic Name
- Arthroscopic shaver system blade, reprocessed FDA UDI
- Device Name
- 280-544-100 @ANGLED AGGRESSIVE PLS CTR ( FDA UDI
- Model / Reference
- UM280544100R FDA UDI
- Description
- 280-544-100 @ANGLED AGGRESSIVE PLS CTR ( FDA UDI
Identifiers
- Catalog Number
- UM280544100R FDA UDI
- Primary DI / UDI-DI
- 10888277373488 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Arthroscopic shaver system blade, reprocessed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 4 Millimeter FDA UDI
Category: Arthroscopic shaver system blade, reprocessed
Medline ReNewal by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Arthroscopic shaver system blade, reprocessed.
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- Sustainable Technologies — Provision · Class II
- Reprocessed 4.0mm Rad 60 Curved Blade, Rotatable — SURETEK MEDICAL · 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 |
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Manufacturer
- Manufacturer
- Medline Industries, Inc.
Sources (1)
- FDA UDI b066c692-3767-47a5-b381-1c314aac831c 36 fields · synced Jun 8, 2026