DEVICE: INSTANT-VIEW Multi-Drugs of Abuse Urine Test AMP, BAR, BZD, COC, MET1000, MOR200 (10796918001358)
Device Identifier (DI) Information
INSTANT-VIEW Multi-Drugs of Abuse Urine Test AMP, BAR, BZD, COC, MET1000, MOR200
03-3916
In Commercial Distribution
ALFA SCIENTIFIC DESIGNS, INC.
03-3916
In Commercial Distribution
ALFA SCIENTIFIC DESIGNS, INC.
INSTANT-VIEW Multi-Drugs of Abuse Urine Test
AMP, BAR, BZD, COC, MET1000, MOR2000,
MTD, PCP, PPX, THC
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| Yes | |
| No | |
| 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? |
|---|---|---|---|---|
| 46996 | Proctological operating table, hydraulic |
A mobile table powered by manually-operated hydraulic mechanisms designed to support a patient during proctological procedures (i.e., diagnosis and treatment of the colon, rectum, anus, and/or the perineum). Its surface consists of sections that can be height-adjusted in relation to the section that supports the patient's trunk and the section supporting the knees (the patient is usually in a kneeling position to provide the surgeon with posterior access).
|
Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| DKE | Reagents, Test, Tetrahydrocannabinol |
| JXN | Enzyme Immunoassay, Propoxyphene |
| LCM | Enzyme Immunoassay, Phencyclidine |
| DJR | Enzyme Immunoassay, Methadone |
| DOE | Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep. |
| DJC | Thin Layer Chromatography, Methamphetamine |
| DIO | Enzyme Immunoassay, Cocaine And Cocaine Metabolites |
| JXM | Enzyme Immunoassay, Benzodiazepine |
| DIS | Enzyme Immunoassay, Barbiturate |
| DKZ | Enzyme Immunoassay, Amphetamine |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| Premarket Submission Number Not Available/Not Released | |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| No storage/handling found |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| No Device Sizes |
Device Record Status
5cd1bf1f-350e-461d-b125-1386bde93957
May 02, 2019
3
September 23, 2016
May 02, 2019
3
September 23, 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 |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
00796918001351
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined