InterCollagen Guide

GUDID 00852072007520

SIGMAGRAFT, INC.

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Primary Device ID00852072007520
NIH Device Record Key774f2da4-da36-4f51-aed9-3914f8690c58
Commercial Distribution StatusIn Commercial Distribution
Brand NameInterCollagen Guide
Version Model NumberICG1520
Company DUNS078893672
Company NameSIGMAGRAFT, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100852072007520 [Primary]

FDA Product Code

NPLBarrier, Animal Source, Intraoral

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-29
Device Publish Date2023-09-21

On-Brand Devices [InterCollagen Guide]

00852072007551ICG3040
00852072007544ICG2525
00852072007537ICG2030
00852072007520ICG1520

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