Identity
- Trade Name
- Responsive Respiratory FDA UDI
- Generic Name
- Nasal oxygen cannula, basic FDA UDI
- Device Name
- Adult Cannula, with 25' Green Safety Tubing FDA UDI
- Model / Reference
- 220-3625 FDA UDI
- Description
- Adult Cannula, with 25' Green Safety Tubing FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851440007643 FDA UDI
- FDA Product Code
- CAT FDA UDI
- GMDN Term
- Nasal oxygen cannula, basic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5340 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Nasal oxygen cannula, basic
Responsive Respiratory by Responsive Respiratory Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nasal oxygen cannula, basic.
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- HUDSON RCI — MEDLINE INDUSTRIES, INC. · Class II
- HUDSON RCI — TELEFLEX INCORPORATED · Class I
- Fisher and Paykel Healthcare — FISHER & PAYKEL HEALTHCARE, INC. · Class II
- BF — Allied Medical LLC · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Responsive Respiratory Inc.
Sources (1)
- FDA UDI 66c2cc63-c120-4a35-ac00-ce2238a16416 33 fields · synced May 30, 2026