Identity
- Trade Name
- Phlebo Press DVT 760D (US) FDA UDI
- Generic Name
- Sequential venous compression system inflator FDA UDI
- Device Name
- The Phlebo Press® DVT system is a pneumatic compression therapy system used to help prevent deep vein thrombosis in patients who may be susceptible. It may also be used to treat conditions as listed in the Indications for Use. The massage action applied by the garments compresses the treated areas to enhance blood flow and reduce stasis. Intermittent and sequential pneumatic compression enhances fibrinolytic activity to reduce the risk of clot formation. FDA UDI
- Model / Reference
- 760D FDA UDI
- Description
- The Phlebo Press® DVT system is a pneumatic compression therapy system used to help prevent deep vein thrombosis in patients who may be susceptible. It may also be used to treat conditions as listed in the Indications for Use. The massage action applied by the garments compresses the treated areas to enhance blood flow and reduce stasis. Intermittent and sequential pneumatic compression enhances fibrinolytic activity to reduce the risk of clot formation. FDA UDI
Identifiers
- Catalog Number
- L10007D4 FDA UDI
- Primary DI / UDI-DI
- 07290105879042 FDA UDI
- 510(k) Number
- K172277 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
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
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Sequential venous compression system inflator
Phlebo Press DVT 760D (US) by MEGO afek Agricultural Cooperative Society Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- MEGO afek Agricultural Cooperative Society Ltd
Sources (1)
- FDA UDI 5b63efc7-1a36-4a3f-b764-147f2e9b6a20 36 fields · synced May 30, 2026