Primary Device ID | 50840200314508 |
NIH Device Record Key | c67448cf-b59a-4819-a72f-6c55df782f64 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | E.M. Adams Company |
Version Model Number | EP28-0301SU-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 | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
emadams@emadamsco.com | |
Phone | 772-461-0532 |
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 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 | 10840200314517 [Primary] |
GS1 | 50840200314508 [Package] Contains: 10840200314517 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 | 2022-05-10 |
Device Publish Date | 2022-05-02 |
50840200314508 | ELBOW SPLINT |
50840200314447 | ELBOW SPLINT |
50840200325313 | SINGLE INSTRUMENT |