Identity
- Trade Name
- EasyStand FDA UDI
- Generic Name
- Manual stander FDA UDI
- Model / Reference
- Evolv Large FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10858921006017 FDA UDI
- 510(k) Number
- K062402 FDA UDI
- FDA Product Code
- INO FDA UDI
- GMDN Term
- Manual stander FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.3110 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Manual standerElectric stander
EasyStand by Altimate Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electric stander.
- EasyStand — Altimate Medical, Inc. · Class II
- EasyStand — Altimate Medical, Inc. · Class II
- EasyStand — Altimate Medical, Inc. · Class II
- EasyStand — Altimate Medical, Inc. · Class I
- EasyStand — Altimate Medical, Inc. · Class II
- EasyStand — Altimate Medical, Inc. · Class II
Cleared under the same submission
K062402 also covers:
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
- Altimate Medical, Inc.
Sources (1)
- FDA UDI 97cfc351-0317-4aa5-8804-bc8fc90d01c6 33 fields · synced Jul 10, 2026