FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Prevena Restor™ Adaptiform™

DI: 00849554008014 · Model: PRE6001 · KCI USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3M™ Prevena Restor™ Adaptiform™
Primary DI
00849554008014
Version / Model
PRE6001
Catalog Number
PRE6001
Company Name
KCI USA, INC.
Labeler DUNS
102726734
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-18
Public Version
1
Public Version Date
2022-08-26
Public Version Status
New
Public Device Record Key
706d3092-c5a2-4f58-b1a5-80aebf20c3c4

Device Description

3M™ Prevena Restor™ Adaptiform™ System Kit

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
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OMP negative pressure wound therapy Powered suction pump

GMDN Terms

Code Name
58202 Negative-pressure wound therapy system, electric, single-use

Identifiers

Type ID
Primary 00849554008014

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K220660 000