Primary Device ID | 08592654348000 |
NIH Device Record Key | b0e34ffd-3675-43f4-b4ab-892e7e5db115 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tom 2 |
Version Model Number | 1K41B511-10 |
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 | 08592654348000 [Primary] |
FMS | Bed, Pediatric Open Hospital |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-08 |
Device Publish Date | 2022-02-28 |
08592654210970 | Pediatric hospital bed. |
08592654345450 | Pediatric hospital bed. |
08592654348000 | Pediatric hospital bed. |
08592654353882 | Pediatric hospital bed. |
08592654289884 | Pediatric hospital bed. |
08592654376386 | Pediatric hospital bed. |
08592654389690 | Pediatric hospital bed. |
08592654351956 | Pediatric hospital bed. |
08592654433973 | Pediatric hospital bed. |