Identity
- Trade Name
- ActiveCare FDA UDI
- Generic Name
- Sequential venous compression system inflator FDA UDI
- Model / Reference
- ActiveCare calf large sleeve with stockinette FDA UDI
Identifiers
- Catalog Number
- A201C220S10 FDA UDI
- Primary DI / UDI-DI
- 00889024504714 FDA UDI
- FDA Product Code
- JOW FDA UDI
- GMDN Term
- Sequential venous compression system inflator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5800 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
Yes
FDA UDI
Category: Sequential venous compression system inflator
ActiveCare by Zimmer Orthopaedic Surgical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
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- Medline — MEDLINE INDUSTRIES, INC. · Class II
- Bio Compression Systems Sequential Circulator Model SC-3008-IS — BIO COMPRESSION SYSTEMS, INC. · Class II
- Air Relax Classic Model AR-2.0 Leg Recovery System - Size 2 — Maxstar Industrial Co., Ltd. · Class II
- TRIPLE PLAY — Compression Solutions, 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
- Zimmer Orthopaedic Surgical Products
Sources (1)
- FDA UDI fcef2dfb-0ed8-4f90-8a22-2484c1ba3bc7 34 fields · synced Jun 8, 2026