Primary Device ID | 50840200320714 |
NIH Device Record Key | 3a124cfb-12f3-4333-bc52-ba75b1047ee8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | E.M. ADAMS CO, INC |
Version Model Number | EP60603XXXXL-1 |
Company DUNS | 001403807 |
Company Name | E.M. ADAMS, INC. |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 7724610532 |
emadams@emadamsco.com | |
Phone | 7724610532 |
emadams@emadamsco.com | |
Phone | 7724610532 |
emadams@emadamsco.com | |
Phone | 7724610532 |
emadams@emadamsco.com | |
Phone | 7724610532 |
emadams@emadamsco.com | |
Phone | 7724610532 |
emadams@emadamsco.com | |
Phone | 7724610532 |
emadams@emadamsco.com | |
Phone | 7724610532 |
emadams@emadamsco.com | |
Phone | 7724610532 |
emadams@emadamsco.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10840200320723 [Primary] |
GS1 | 50840200320714 [Package] Contains: 10840200320723 Package: Case [6 Units] In Commercial Distribution |
FMQ | Restraint, Protective |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-25 |
Device Publish Date | 2022-07-17 |