FDA UDI In Commercial Distribution 🇺🇸 United States

ProCure

DI: 10840330701737 · Model: PCKDK20 · Twin Med, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ProCure
Primary DI
10840330701737
Version / Model
PCKDK20
Catalog Number
PCKDK20
Company Name
Twin Med, LLC
Labeler DUNS
107071289
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-31
Public Version
2
Public Version Date
2026-04-07
Public Version Status
Update
Public Device Record Key
4a8ede7e-1984-42c6-bba0-920262ab2009

Device Description

Debridement Kit Sterile 20ea/cs

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
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
KDD Kit, Surgical Instrument, Disposable

GMDN Terms

Code Name
34059 Wound dressing kit, medicated

Identifiers

Type ID
Package 30840330701731
Primary 10840330701737

Customer Contacts

Phone
804-776-2873