Primary Device ID | 00850021303129 |
NIH Device Record Key | 845b1c4c-7394-474f-acf2-0b715abaf29a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Activator Methods |
Version Model Number | ARIV Blue |
Company DUNS | 194879383 |
Company Name | Activator Methods International, Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
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 | 00850021303129 [Primary] |
LXM | Manipulator, Plunger-Like Joint |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-26 |
Device Publish Date | 2020-10-16 |
00850021303136 | Chiropractic Adjusting Instrument |
00850021303129 | Chiropractic Adjusting Instrument |
00850021303112 | Chiropractic Adjusting Instrument |
00850021303105 | Chiropractic Adjusting Instrument |
00850021303099 | Chiropractic Adjusting Instrument |
00850021303082 | Chiropractic Adjusting Instrument |
00850021303051 | Chiropractic Adjusting Instrument |
00850021303044 | Chiropractic Adjusting Instrument |
00850021303020 | Chiropractic Adjusting Instrument |
00850021303013 | Chiropractic Adjusting Instrument |
00850021303006 | Chiropractic Adjusting Instrument |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACTIVATOR METHODS 76061062 2467750 Dead/Cancelled |
Activator Methods International, Ltd. 2000-06-01 |
ACTIVATOR METHODS 73539873 1379670 Live/Registered |
ACTIVATOR METHODS, INC. 1985-05-28 |