FDA UDI In Commercial Distribution 🇺🇸 United States

ClearPetra

DI: 06944932740273 · Model: 90131821 · Well Lead Medical Co.,Ltd
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ClearPetra
Primary DI
06944932740273
Version / Model
90131821
Company Name
Well Lead Medical Co.,Ltd
Labeler DUNS
544811862
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-04
Public Version
1
Public Version Date
2020-12-14
Public Version Status
New
Public Device Record Key
c68aefc2-8668-49b6-b2aa-065e697b8ae4

Device Description

ClearPetra Cystoscope Sheath, 18Fr×21cm

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FED Endoscopic Access Overtube, Gastroenterology-Urology
FAJ Cystoscope And Accessories, Flexible/Rigid
FGA Kit, Nephroscope

GMDN Terms

Code Name
63564 Endoscope sheath, single-use

Identifiers

Type ID
Package 16944932740270
Primary 06944932740273
Package 26944932740277

Premarket Submissions

Submission Number Supplement Number
K161110 000