KerraPro KPRO60

GUDID 05060077234123

CRAWFORD HEALTHCARE LIMITED

Pressure-management bandage, silicone
Primary Device ID05060077234123
NIH Device Record Keyf7898ae0-6391-49be-91ae-f17d9a1c149d
Commercial Distribution StatusIn Commercial Distribution
Brand NameKerraPro
Version Model Number20 x 1 x 0.1in
Catalog NumberKPRO60
Company DUNS543740310
Company NameCRAWFORD HEALTHCARE LIMITED
Device Count1
DM Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com
Phone+4401565654920
Emailandrew.jackson@acelity.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105060077230637 [Primary]
GS105060077230644 [Package]
Contains: 05060077230637
Package: Carton [5 Units]
In Commercial Distribution
GS105060077234123 [Package]
Contains: 05060077230644
Package: Shipper [32 Units]
In Commercial Distribution

FDA Product Code

FMPProtector, Skin Pressure

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-10-09
Device Publish Date2019-10-01

On-Brand Devices [KerraPro]

0506007723412320 x 1 x 0.1in
0506007723411612 x 2 x 0.1in
050600772303924 x 4 x 0.5in
050600772340934 x 4 x 0.1 in
05060077234086Heel

Trademark Results [KerraPro]

Mark Image

Registration | Serial
Company
Trademark
Application Date
KERRAPRO
KERRAPRO
85700570 4449859 Live/Registered
SYSTAGENIX WOUND MANAGEMENT, LIMITED
2012-08-10

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