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TEVADAPTOR® Secondary IV Administration Set with ULTRASITE® Inj. Site
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- TEVADAPTOR® Secondary IV Administration Set with ULTRASITE® Inj. Site FDA UDI
- Generic Name
- Basic intravenous administration set, noninvasive FDA UDI
- Device Name
- TEVADAPTOR® Secondary IV Administration Set with ULTRASITE® Injection Site for use with OnGuardTM contained Medication System FDA UDI
- Model / Reference
- MG412120 FDA UDI
- Description
- TEVADAPTOR® Secondary IV Administration Set with ULTRASITE® Injection Site for use with OnGuardTM contained Medication System FDA UDI
Identifiers
- Catalog Number
- MG412120 FDA UDI
- Primary DI / UDI-DI
- 27298119121205 FDA UDI
- 510(k) Number
- K121269 FDA UDI
- FDA Product Code
- FPA FDA UDI
- GMDN Term
- Basic intravenous administration set, noninvasive FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 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
Yes
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
No
FDA UDI
Category: Basic intravenous administration set, noninvasive
TEVADAPTOR® Secondary IV Administration Set with ULTRASITE® Inj. Site by Teva Pharmaceutical Industries Limited — Class II — FDA UDI — listed in FDA GUDID
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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
- Teva Pharmaceutical Industries Limited
Sources (1)
- FDA UDI 1080b927-217c-484c-9367-54502bfd252d 35 fields · synced May 31, 2026