Primary Device ID | 00850001456227 |
NIH Device Record Key | 0a6684ed-c811-4d44-a6f4-2bb1a9c73003 |
Commercial Distribution Discontinuation | 2030-11-20 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AECOR200 - Neck |
Version Model Number | AE200 |
Company DUNS | 010000704 |
Company Name | Omm Imports 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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850001456227 [Primary] |
ISA | Massager, Therapeutic, Electric |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-22 |
Device Publish Date | 2022-06-14 |
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