Primary Device ID | B303E040 |
NIH Device Record Key | 408c295d-1f78-42a2-b812-1eb21524a1d2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VersaTech 700 ULB |
Version Model Number | V7ULB+-xx-1000 |
Company DUNS | 245707815 |
Company Name | Usine Rotec 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 | 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 |
---|---|
HIBCC | B303E040 [Primary] |
FNL | Bed, Ac-Powered Adjustable 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 | 2025-04-21 |
Device Publish Date | 2025-04-11 |
B303D040 - VersaTech 1100 ULB | 2025-04-21 |
B303D041 - VersaTech 1100 ULB+ | 2025-04-21 |
B303D042 - VersaTech 1100 ULB+ | 2025-04-21 |
B303E030 - VersaTech 600 ULB | 2025-04-21 |
B303E031 - VersaTech 600 ULB+ | 2025-04-21 |
B303E040 - VersaTech 700 ULB | 2025-04-21 |
B303E040 - VersaTech 700 ULB | 2025-04-21 |
B303E041 - VersaTech 700 ULB+ | 2025-04-21 |
B303E042 - VersaTech 700 ULB+ | 2025-04-21 |