Identity
- Trade Name
- HUDSON RCI FDA UDI
- Generic Name
- Inhalation therapy sterile water FDA UDI
- Device Name
- AQUAPAK Sterile Water for Inhalation 1070 mL w/ 033 Nebulizer Adaptor FDA UDI
- Model / Reference
- IPN044359 FDA UDI
- Description
- AQUAPAK Sterile Water for Inhalation 1070 mL w/ 033 Nebulizer Adaptor FDA UDI
Identifiers
- Catalog Number
- 404133 FDA UDI
- Primary DI / UDI-DI
- 14026704611307 FDA UDI
- FDA Product Code
- OGG FDA UDI
- GMDN Term
- Inhalation therapy sterile water FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5450 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
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
No
FDA UDI
Category: Inhalation therapy sterile water
Hudson Rci by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- HUDSON RCI — MEDLINE INDUSTRIES, INC. · Class II
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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
- Teleflex Incorporated
Sources (1)
- FDA UDI 2f6d9c3f-e306-431c-93b1-044743e962ea 36 fields · synced May 30, 2026