DEVICE: OPTIGEN® Allergen-Specific IgE Assay - US Inhalant 36(100 ND) (00813382010426)
Device Identifier (DI) Information
OPTIGEN® Allergen-Specific IgE Assay - US Inhalant 36(100 ND)
85081
In Commercial Distribution
85081
Minaris Medical America, Inc.
85081
In Commercial Distribution
85081
Minaris Medical America, Inc.
KIT, OPTIGEN US Inhalant 36 (100 ND)
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| Yes | |
| Yes | |
| No | |
| Yes | |
| 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? |
|---|---|---|---|---|
| 61955 | Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, chemiluminescent immunoassay |
A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin E (IgE) antibodies to one or multiple allergen(s) in a clinical specimen, using a chemiluminescent immunoassay method. It is typically used to screen for allergies associated with certain conditions (e.g., food intolerance).
|
Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| PUW | System, test, radioallergosorbent (Rast) immunological, exempt allergens |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| Premarket Submission Number Not Available/Not Released | |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Storage Environment Temperature: between 2 and 10 Degrees Celsius |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| No Device Sizes |
Device Record Status
cebb3ff1-526f-40bf-ac13-33edf457f57b
August 03, 2023
4
May 22, 2019
August 03, 2023
4
May 22, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
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(650)961-5501
686
info@hcdiagnostics.com
info@hcdiagnostics.com