SurCura Antibacterial Wound Matrix

GUDID 06977727072419

SurCura Antibacterial Wound Matrix is a sterile,single-use device intended for use in the management of wounds.

Beijing Kreate Medical Co., Ltd.

Synthetic wound matrix dressing
Primary Device ID06977727072419
NIH Device Record Key837c4504-3db5-4154-b5b7-0b8f87e5f78d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSurCura Antibacterial Wound Matrix
Version Model NumberSCAB-55D
Company DUNS843094168
Company NameBeijing Kreate Medical Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106977727072419 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRODressing, Wound, Drug

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-31
Device Publish Date2026-03-23

On-Brand Devices [SurCura Antibacterial Wound Matrix]

06977727072440SurCura Antibacterial Wound Matrix is a sterile,single-use device intended for use in the manage
06977727072433SurCura Antibacterial Wound Matrix is a sterile,single-use device intended for use in the manage
06977727072426SurCura Antibacterial Wound Matrix is a sterile,single-use device intended for use in the manage
06977727072419SurCura Antibacterial Wound Matrix is a sterile,single-use device intended for use in the manage

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.