DEVICE: neria multi (05705244002197)
Device Identifier (DI) Information
neria multi
721060-4731
Not in Commercial Distribution
Unomedical A/S
721060-4731
Not in Commercial Distribution
Unomedical A/S
Single use infusion set for subcutaneous infusion. The infusion set must be used as described in the Instruction for Use.
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
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? |
---|---|---|---|---|
35833 | Electric infusion pump administration set, single-use |
A collection of sterile devices (e.g., plastic tubing, check valve, roller clamp, Y-site connector, Luer, needle/catheter) intended to be used in combination with an electrically-powered infusion pump for the intravenous (IV), subcutaneous, intramuscular, or epidural administration of medication. This is a single-use device.
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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: Protect from direct sunlight. Store at room temperature |
Clinically Relevant Size
[?]Size Type Text |
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Device Size Text, specify: Length 60+30 cm |
Depth: 10 Millimeter |
Angle: 90 degree |
Device Record Status
78208853-a9e0-4db6-b86f-5bfcc3d24cab
May 10, 2024
5
September 15, 2016
May 10, 2024
5
September 15, 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 |
---|---|---|---|---|---|
05705244002203 | 120 | 05705244002197 | 2024-05-09 | Not in Commercial Distribution | Outer box |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
05705244010277
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined