Primary Device ID | 08592654356678 |
NIH Device Record Key | ce6b83ea-15a8-46ea-99e6-5416d814b1e3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sprint 200 |
Version Model Number | 1ES211-1 |
Company DUNS | 644544504 |
Company Name | L I N E T spol. s r.o. |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
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 | 08592654356678 [Primary] |
INK | Stretcher, Wheeled, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-18 |
Device Publish Date | 2022-11-10 |
08592654358467 | The sprint stretcher transport bed. |
08592654356685 | The sprint stretcher transport bed with scales. |
08592654356678 | The sprint stretcher transport bed with scales. |
08592654390894 | The sprint stretcher transport bed with scales. |
08592654389102 | The sprint stretcher transport bed with scales. |
08592654407868 | The sprint stretcher transport bed with scales. |