Primary Device ID | 10816317023475 |
NIH Device Record Key | ec91aad9-f686-4014-9c69-5a2b7d446f1c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sage Lateral Transfer Mat |
Version Model Number | RM-7219 |
Company DUNS | 100439103 |
Company Name | RENU MEDICAL, INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816317023478 [Primary] |
GS1 | 10816317023475 [Package] Contains: 00816317023478 Package: Case [10 Units] In Commercial Distribution |
FMR | Device, Transfer, Patient, Manual |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-07 |
Device Publish Date | 2023-06-29 |
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