Identity
- Trade Name
- Responsive Respiratory, Inc. FDA UDI
- Generic Name
- Anaesthesia/respiratory gas flowmeter tester FDA UDI
- Device Name
- Liter Meter, 0-2.5 LPM FDA UDI
- Model / Reference
- 180-5004 FDA UDI
- Description
- Liter Meter, 0-2.5 LPM FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851440007599 FDA UDI
- FDA Product Code
- BXY FDA UDI
- GMDN Term
- Anaesthesia/respiratory gas flowmeter tester FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.2350 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
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Anaesthesia/respiratory gas flowmeter tester
Responsive Respiratory, Inc. by Responsive Respiratory Inc. — 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
- Responsive Respiratory Inc.
Sources (1)
- FDA UDI fa2c2ac2-3aee-4794-acf7-1ede13ec9f6e 33 fields · synced May 30, 2026