DEVICE: neria™ guard (05705244022355)
Device Identifier (DI) Information
neria™ guard
704110-5229
Not in Commercial Distribution
Unomedical A/S
704110-5229
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.
|
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: Store the product at room temperature. Keep the product away from direct sunlight and any humid environment. |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Length: 110 Centimeter |
| Depth: 9 Millimeter |
| Angle: 90 degree |
Device Record Status
355be57f-9517-42ef-82f9-3964031a330d
May 10, 2024
6
January 24, 2020
May 10, 2024
6
January 24, 2020
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| 05705244022362 | 80 | 05705244022355 | 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:
05705244022379
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
9999999999
xx@xx.xx
xx@xx.xx