| Primary Device ID | 00766588620343 |
| NIH Device Record Key | 893793ba-30e9-4e21-8274-dd422b2dcd87 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 75H - Class A MRO 21 - w/Select Logo |
| Version Model Number | K622-034 |
| Catalog Number | K622-034 |
| Company DUNS | 788460483 |
| Company Name | Certified Safety Manufacturing, 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 | true |
| Device Combination Product | true |
| Single Use | true |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +1(816)483-9090 |
| Info@certifiedsafety.com | |
| Phone | +1(816)483-9090 |
| Info@certifiedsafety.com | |
| Phone | +1(816)483-9090 |
| Info@certifiedsafety.com | |
| Phone | +1(816)483-9090 |
| Info@certifiedsafety.com | |
| Phone | +1(816)483-9090 |
| Info@certifiedsafety.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00766588620343 [Primary] |
| LRR | First Aid Kit with drug |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-08 |
| Device Publish Date | 2022-10-31 |
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