FDA UDI Not in Commercial Distribution 🇺🇸 United States

3C Patch® Device

DI: 05714188502151 · Model: 1 · Reapplix ApS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3C Patch® Device
Primary DI
05714188502151
Version / Model
1
Company Name
Reapplix ApS
Labeler DUNS
312293991
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-19
Public Version
4
Public Version Date
2023-01-03
Public Version Status
Update
Public Device Record Key
bd63355d-596d-4c50-858c-0cf676919311
Distribution End Date
2020-01-02

Device Description

Holds the blood at collection and during processing in the centrifuge.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PMQ Peripheral Blood Processing Device For Wound Management

GMDN Terms

Code Name
46923 Haematological concentrate system preparation kit, platelet concentration

Identifiers

Type ID
Primary 05714188502151

Customer Contacts

Phone
+4588168066