Primary Device ID | B21257112 |
NIH Device Record Key | 1298c248-e361-4779-9b86-4ff69c694fca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Female Syringe Luer Cap |
Version Model Number | 57-11 |
Catalog Number | 57-11 |
Company DUNS | 053469565 |
Company Name | INTERNATIONAL MEDICAL INDUSTRIES 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B21257111 [Primary] |
HIBCC | B21257112 [Package] Contains: B21257111 Package: Box [100 Units] In Commercial Distribution |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-23 |
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