FDA UDI In Commercial Distribution 🇺🇸 United States

MediClear™ PreOp

DI: 00825439012871 · Model: 7000607 · Covalon Technologies Ltd
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MediClear™ PreOp
Primary DI
00825439012871
Version / Model
7000607
Company Name
Covalon Technologies Ltd
Labeler DUNS
206936101
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-30
Public Version
6
Public Version Date
2022-12-02
Public Version Status
Update
Public Device Record Key
f5ec0d15-e53d-42a7-8845-6ca57bf3bee0

Device Description

Antimicrobial Self-Adherent Silicone Film Drape for PreOperative Skin with Chlorhexidine and Silver

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Safe
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
KKX Drape, Surgical

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Primary 00825439012871
Package 00825439012888
Package 10825439012892

Premarket Submissions

Submission Number Supplement Number
K163556 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 6cm x 7cm (2.4in x 2.8in)