FDA UDI In Commercial Distribution 🇺🇸 United States

MediClear PreOp

DI: 00825439012819 · Model: 7000630 · Covalon Technologies Ltd
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MediClear PreOp
Primary DI
00825439012819
Version / Model
7000630
Company Name
Covalon Technologies Ltd
Labeler DUNS
206936101
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-01
Public Version
1
Public Version Date
2022-12-09
Public Version Status
New
Public Device Record Key
361c556d-601a-4b75-b456-c45f7107fbc7

Device Description

Antimicrobial silicone film drape

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
Package 00825439012826
Primary 00825439012819
Package 10825439012830

Premarket Submissions

Submission Number Supplement Number
K163556 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 6x30 cm

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 25 Degrees Celsius