Identity
- Trade Name
- Rapid Reboot FDA UDI
- Generic Name
- Intermittent venous compression system FDA UDI
- Model / Reference
- SP-H1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B691SPH10 FDA UDI
- FDA Product Code
- IRP FDA UDI
- GMDN Term
- Intermittent venous compression system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5650 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
Yes
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
No
FDA UDI
Category: Intermittent venous compression systemSequential venous compression system
Rapid Reboot by Rapid Reboot Recovery Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Sequential venous compression system.
- Pulse Boot Set — NORMATEC INDUSTRIES, LP · Class II
- Blue Boot — NORMATEC INDUSTRIES, LP · Class II
- Mueller Sports Medicine — Mueller Sports Medicine, Inc. · Class II
- HYDROVEN — Huntleigh Healthcare , Ltd. · Class II
- AeroWrap™ Flex Large — SUN-SCIENTIFIC INC. · Class I
- Pulse Carry Case — NORMATEC INDUSTRIES, LP · Class II
- Pulse Boot — NORMATEC INDUSTRIES, LP · Class II
- CoreTech — VIVE HEALTH 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Rapid Reboot Recovery Products
Sources (1)
- FDA UDI 8d54c6a8-8e95-4b4f-bbfd-90314f313b36 32 fields · synced May 30, 2026