Primary Device ID | 10884521844292 |
NIH Device Record Key | 99a13108-6be7-4cea-a5ad-fb55e01e75a6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProGrip |
Version Model Number | PP3020G |
Company DUNS | 576342646 |
Company Name | SOFRADIM PRODUCTION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Width | 20 Centimeter |
Length | 30 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884521844292 [Primary] |
FTL | Mesh, surgical, polymeric |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-12 |
Device Publish Date | 2024-02-04 |
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