Primary Device ID | 20817120020290 |
NIH Device Record Key | 4f1cfd4d-9c2d-4cb0-bb5e-8819ff01d1eb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bio Protech |
Version Model Number | 9552F |
Company DUNS | 789127011 |
Company Name | BIO PROTECH USA, INC. |
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 | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 714-730-9950 |
bioprotechusa@gmail.com | |
Phone | 714-730-9950 |
bioprotechusa@gmail.com | |
Phone | 714-730-9950 |
bioprotechusa@gmail.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817120020296 [Primary] |
GS1 | 10817120020293 [Package] Contains: 00817120020296 Package: Inner Box [40 Units] Discontinued: 2017-06-06 Not in Commercial Distribution |
GS1 | 20817120020290 [Package] Contains: 10817120020293 Package: Master Case [2 Units] Discontinued: 2017-06-06 Not in Commercial Distribution |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-06-28 |
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