Primary Device ID | B5331181201 |
NIH Device Record Key | e076f954-3350-4836-8dfd-187111d9314f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | JK-RUSA |
Version Model Number | 400 R7s |
Catalog Number | 118120 |
Company DUNS | 315736603 |
Company Name | BLV Licht- und Vakuumtechnik GmbH |
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 | false |
Device Combination Product | false |
Single Use | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B5331081960 [Previous] |
HIBCC | B5331181200 [Primary] |
HIBCC | B5331181201 [Package] Contains: B5331181200 Package: Carton box [25 Units] In Commercial Distribution |
HIBCC | B5331181202 [Package] Contains: B5331181200 Package: Carton box [50 Units] In Commercial Distribution |
LEJ | Booth, Sun Tan |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-04 |
Device Publish Date | 2023-07-27 |
B5331081961 | 400W R7s |
B5331181201 | 400 R7s |