Identity
- Trade Name
- MAXBLEND 2 FDA UDI
- Generic Name
- Anaesthesia/respiratory gas flowmeter tester FDA UDI
- Model / Reference
- R229P01-010 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817770021094 FDA UDI
- FDA Product Code
- BZR FDA UDI
- GMDN Term
- Anaesthesia/respiratory gas flowmeter tester FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5330 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Anaesthesia/respiratory gas flowmeter tester
Maxblend 2 by Maxtec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Anaesthesia/respiratory gas flowmeter tester.
- Responsive Respiratory, Inc. — RESPONSIVE RESPIRATORY INC. · Class I
- Flow Analyzer PF-300 PRO — IMT ANALYTICS INC. · Class I
- Flow Analyzer PF-300 — IMT ANALYTICS INC. · Class I
- Responsive Respiratory, Inc. — RESPONSIVE RESPIRATORY INC. · Class I
- CITREX H4 — IMT ANALYTICS INC. · Class I
- FlowMeter F1 — IMT ANALYTICS INC. · Class I
- CITREX H3 — IMT ANALYTICS INC. · Class I
- Responsive Respiratory, Inc. — RESPONSIVE RESPIRATORY INC. · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Maxtec, Inc.
Sources (1)
- FDA UDI 03c941df-d43f-4164-a4ef-33ccf56fcd1b 32 fields · synced May 31, 2026