Identity
- Trade Name
- Ohio Medical Vacuum Regulator FDA UDI
- Generic Name
- Vacuum suction regulator/regulation set, general-purpose FDA UDI
- Device Name
- Vacuum Regulator, Push to Set, Continuous 3 Mode, 760mmHg Analog FDA UDI
- Model / Reference
- PC3HA FDA UDI
- Description
- Vacuum Regulator, Push to Set, Continuous 3 Mode, 760mmHg Analog FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08688250002122 FDA UDI
- FDA Product Code
- KDP FDA UDI
- GMDN Term
- Vacuum suction regulator/regulation set, general-purpose FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Ohio Medical Vacuum Regulator by Ohio Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Ohio Medical LLC
Sources (1)
- FDA UDI 15603901-3b14-46d4-8d75-5b4d08061366 35 fields · synced May 31, 2026