Genemed® 60-0222-15

GUDID 00615233008190

anti-Procollagen-1 Rat Monoclonal Antibody [M-58], Ready-To-Use, 15 mL

SAKURA FINETEK U.S.A., INC.

Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control Procollagen type I N-terminal propeptide (PINP) IVD, control
Primary Device ID00615233008190
NIH Device Record Keyba19b2f6-f2ea-462f-81f5-9825b328f26e
Commercial Distribution StatusIn Commercial Distribution
Brand NameGenemed®
Version Model Number60-0222-15
Catalog Number60-0222-15
Company DUNS179135769
Company NameSAKURA FINETEK U.S.A., INC.
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com
Phone+1(310)972-7800
EmailTS@sakuraus.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]
GS100615233008190 [Primary]

FDA Product Code

MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte
MVUReagents, specific, analyte

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-14
Device Publish Date2020-09-05

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