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Pressure Monitoring Line with Nafion Dryer (BioMed Private Label)
FDA UDIClass II (US FDA UDI)
by Maxtec, Inc.
Identity
- Trade Name
- Pressure Monitoring Line with Nafion Dryer (BioMed Private Label) FDA UDI
- Generic Name
- Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
- Device Name
- Pressure Monitoring Line with Nafion Dryer (BioMed Private Label) - SINGLE, EACHES LEVEL FDA UDI
- Model / Reference
- R229P18-001 FDA UDI
- Description
- Pressure Monitoring Line with Nafion Dryer (BioMed Private Label) - SINGLE, EACHES LEVEL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817770026068 FDA UDI
- FDA Product Code
- CBQ FDA UDI
- GMDN Term
- Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Gas-sampling/monitoring respiratory tubing, single-use
Pressure Monitoring Line with Nafion Dryer (BioMed Private Label) by Maxtec, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Maxtec, Inc.
Sources (1)
- FDA UDI d5e1650b-e419-498f-a858-8f08b9907dbc 33 fields · synced May 30, 2026