Identity
- Trade Name
- Midmark FDA UDI
- Generic Name
- Dental suction system FDA UDI
- Device Name
- Midmark PowerAir Oil-Less Compressors, with sound cover, are intended to provide compressed air during general examinations and procedures conducted by qualified dental professionals. Model: P52SC, Number of users: 5 - 7, Number of heads: 2, Total HP: 3.2, CFM @ 80psi: 10.6, Voltage: 208 - 230. Midmark PowerVac Dry vacuums are intended to provide suction during general examinations and procedures conducted by qualified dental professionals. Model: P5, Number of users: 5 - 7, Number of vacuums: 1, Total HP: 2. FDA UDI
- Model / Reference
- P52SC/P5 FDA UDI
- Description
- Midmark PowerAir Oil-Less Compressors, with sound cover, are intended to provide compressed air during general examinations and procedures conducted by qualified dental professionals. Model: P52SC, Number of users: 5 - 7, Number of heads: 2, Total HP: 3.2, CFM @ 80psi: 10.6, Voltage: 208 - 230. Midmark PowerVac Dry vacuums are intended to provide suction during general examinations and procedures conducted by qualified dental professionals. Model: P5, Number of users: 5 - 7, Number of vacuums: 1, Total HP: 2. FDA UDI
Identifiers
- Catalog Number
- P52SC/P5 FDA UDI
- Primary DI / UDI-DI
- 00841709108662 FDA UDI
- FDA Product Code
- NRD FDA UDI
- GMDN Term
- Dental suction system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6640 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
No
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
Yes
FDA UDI
Category: Dental suction systemMedical device air compressor
Midmark by Midmark Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Midmark Corporation
Sources (1)
- FDA UDI 7854fb18-1b21-47f8-8c56-8660c7cb370b 36 fields · synced Jun 8, 2026