Identity
- Trade Name
- 3CP™ Counterbalance FDA UDI
- Generic Name
- Centrifuge tube counterbalance FDA UDI
- Device Name
- Used with 3CP Centrifuge to counterbalance weight of 3C Patch Device(s). FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- Used with 3CP Centrifuge to counterbalance weight of 3C Patch Device(s). FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05714188301822 FDA UDI
- FDA Product Code
- PMQ FDA UDI
- GMDN Term
- Centrifuge tube counterbalance FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.9245 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
3CP™ Counterbalance by Reapplix ApS — 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
- Reapplix ApS
Sources (1)
- FDA UDI 3ee0ca66-47a5-49f4-9cb0-2c4702cd7e67 35 fields · synced May 30, 2026