| Primary Device ID | 50840200323395 |
| NIH Device Record Key | 41430ec2-0dd7-453a-9741-8d52f56f0f39 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | E.M. Adams Co, Inc. |
| Version Model Number | EP90401L-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 |
| 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 | 10840200323403 [Primary] |
| GS1 | 50840200323395 [Package] Contains: 10840200323403 Package: Case [24 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 | 2022-05-26 |
| Device Publish Date | 2022-05-18 |