Identity
- Trade Name
- Patient Administration Set FDA UDI
- Generic Name
- Radioaerosol administration set FDA UDI
- Model / Reference
- None FDA UDI
Identifiers
- Catalog Number
- 17836 FDA UDI
- Primary DI / UDI-DI
- 09340598000091 FDA UDI
- FDA Product Code
- IYT FDA UDI
- GMDN Term
- Radioaerosol administration set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1390 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Radioaerosol administration set
Patient Administration Set by Cyclomedica Australia Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Radioaerosol administration set.
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- Aero/Vent Plus — MEDI NUCLEAR CORP., INC. · Class II
- Insta/Vent — MEDI NUCLEAR CORP., INC. · Class II
- Aerotech I Radioaerosol Administration System — Biodex Medical Systems · Class II
- Aero/Vent Jr. — MEDI NUCLEAR CORP., INC. · Class II
- Insta/Vent — MEDI NUCLEAR CORP., INC. · Class II
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
- Cyclomedica Australia Pty Ltd
Sources (1)
- FDA UDI 2d1c57f6-54e9-4cd0-9d37-6992573a5736 33 fields · synced Jun 1, 2026