Identity
- Trade Name
- Hospira FDA UDI
- Generic Name
- Bedside infusion pump, single-channel FDA UDI
- Device Name
- LIFESHIELD LATEX FREE SOLUSET 150ML BURETTE, CONVERTIBLE PIERCING PIN DUAL CHANNEL 4 CLAVE PORTS IN LINE CHECK VALVE, OPTION LOK NON-DEHP FDA UDI
- Model / Reference
- 1972128 FDA UDI
- Description
- LIFESHIELD LATEX FREE SOLUSET 150ML BURETTE, CONVERTIBLE PIERCING PIN DUAL CHANNEL 4 CLAVE PORTS IN LINE CHECK VALVE, OPTION LOK NON-DEHP FDA UDI
Identifiers
- Catalog Number
- 1972128 FDA UDI
- Primary DI / UDI-DI
- 10887787008934 FDA UDI
- FDA Product Code
- FPA FDA UDI
- GMDN Term
- Bedside infusion pump, single-channel 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
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
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
Dimensions & Sizes
- Size
- Length — 145 Inch FDA UDI
Category: Bedside infusion pump, single-channel
Hospira by Hospira, Inc. — 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
- Hospira, Inc.
Sources (1)
- FDA UDI 17f4e099-ceb3-43b0-852d-55904c09922d 37 fields · synced May 30, 2026