Primary Device ID | 00850053135156 |
NIH Device Record Key | 7a2bffaf-d050-4265-8b67-dde8e25098ec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BH Supplies |
Version Model Number | BH1LS |
Company DUNS | 038516520 |
Company Name | Anrel Distribution LLC |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 00850053135156 [Primary] |
FMF | Syringe, Piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-13 |
Device Publish Date | 2023-11-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BH SUPPLIES 88759405 not registered Live/Pending |
Anr Trade LLC 2020-01-15 |