Primary Device ID | 00082161404125 |
NIH Device Record Key | 24f6dab4-bc49-4932-9700-320b8cc8ac14 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spark |
Version Model Number | 40412 |
Company DUNS | 091999771 |
Company Name | BROWNMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00082161404125 [Primary] |
ISY | Joint, Knee, External Limb Component |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-26 |
Device Publish Date | 2020-08-18 |
00082161404286 | Spark Kinetic Ankle |
00082161404279 | Spark Kinetic Ankle |
00082161404262 | Spark Kinetic Ankle |
00082161404187 | Spark Kinetic Elbow |
00082161404170 | Spark Kinetic Elbow |
00082161404163 | Spark Kinetic Elbow |
00082161404125 | Spark Kinetic Knee |
00082161404118 | Spark Kinetic Knee |
00082161404101 | Spark Kinetic Knee |
00082161404224 | Spark Kinetic Calf |
00082161404217 | Spark Kinetic Calf |
00082161404200 | Spark Kinetic Calf |