Cramer Blister Derm

GUDID 10311960560617

Cramer Blister Derm, Dressing, Wound, Hydrogel W/Out Drug And/Or Biologic

CRAMER PRODUCTS, INC.

Wound hydrogel dressing, non-sterile
Primary Device ID10311960560617
NIH Device Record Key2b2d0038-57a0-404f-bb08-79ea322e27fa
Commercial Distribution StatusIn Commercial Distribution
Brand NameCramer Blister Derm
Version Model Number030905
Company DUNS007138183
Company NameCRAMER PRODUCTS, INC.
Device Count20
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Dimensions

Circumference3 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100311960560610 [Primary]
GS110311960560617 [Package]
Contains: 00311960560610
Package: Master Carton [12 Units]
In Commercial Distribution
GS120311960560614 [Unit of Use]

FDA Product Code

NAEDressing, Wound, Hydrogel Without Drug And/Or Biologic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-11-01
Device Publish Date2018-10-01

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