Identity
- Trade Name
- CONMED FDA UDI
- Generic Name
- Intravenous pressure infusor, automated FDA UDI
- Device Name
- 3 LITER PRESSURE INFUSOR FDA UDI
- Model / Reference
- 270165 FDA UDI
- Description
- 3 LITER PRESSURE INFUSOR FDA UDI
Identifiers
- Catalog Number
- 270165 FDA UDI
- Primary DI / UDI-DI
- 30653405040945 FDA UDI
- 510(k) Number
- K980089 FDA UDI
- FDA Product Code
- FRN FDA UDI
- GMDN Term
- Intravenous pressure infusor, automated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Intravenous pressure infusor, automated
Conmed by Conmed Corporation — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI dc1e94cf-edc2-4f4a-9d08-d11fe3c6bf24 37 fields · synced May 30, 2026