Primary Device ID | 00860177000636 |
NIH Device Record Key | e25a9c07-a77c-4392-966c-3fb877913466 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Max Pro Medical Freeze Spray |
Version Model Number | MPMF-6567 |
Company DUNS | 121411859 |
Company Name | ECOTEC MANUFACTURING, 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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860177000636 [Primary] |
IFI | Sprays, Synthetic, Smear |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-17 |
Device Publish Date | 2018-08-15 |
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00860177000636 - Max Pro Medical Freeze Spray | 2018-09-17Medical Freeze Spray |
00860177000636 - Max Pro Medical Freeze Spray | 2018-09-17 Medical Freeze Spray |