DEVICE: Plum (10887787008897)
Device Identifier (DI) Information
Plum
1968528
In Commercial Distribution
1968528
HOSPIRA, INC.
1968528
In Commercial Distribution
1968528
HOSPIRA, INC.
LIFESHIELD LATEX-FREE PLUMSET PRIMARY PIERCING PIN W/SIGHT CHAMBER, THREE WAY STOPCOCK, CLAVE PORTS, OPTION-LOK, NON-DEHP
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
Yes | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
13215 | Bedside infusion pump, single-channel |
An electrically-powered, non-ambulatory (bedside) device designed to facilitate the accurate and consistent administration of a single drug/solution which can be delivered via intravenous, subcutaneous, arterial, epidural, and intracavital routes using a dedicated infusion set; it is not dedicated to a specific treatment type. It is used to supply higher pressures than those provided by gravity infusion sets or infusion controllers (e.g., typical flow range of 1 to 999 ml/hour) and delivers solutions from a standard infusion bag or bottle of fluid. It is intended primarily for use at the bedside but typically has internal batteries that enable operation, e.g., during transportation.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
FPA | Set, administration, intravascular |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
Special Storage Condition, Specify: Room Temperature. Avoid Excessive Heat. Protect from Freezing |
Clinically Relevant Size
[?]Size Type Text |
---|
Length: 136 Inch |
Device Size Text, specify: Approximate priming volume : 24 Milliliter |
Device Size Text, specify: Drop Size : 15 Drops / Milliliter |
Device Record Status
f8100900-ac03-410f-afaf-35f2948eafa2
July 04, 2022
4
September 01, 2016
July 04, 2022
4
September 01, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
20887787008894 | 48 | 10887787008897 | In Commercial Distribution | case |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
HIBCC | M33519685281 |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(877)946-7747
uscustomercare@pfizer.com
uscustomercare@pfizer.com