FDA UDI In Commercial Distribution 🇺🇸 United States

ZKSK

DI: 06934415023337 · Model: HE40-195-2 · Beijing ZKSK Technology Co.,Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZKSK
Primary DI
06934415023337
Version / Model
HE40-195-2
Company Name
Beijing ZKSK Technology Co.,Ltd
Labeler DUNS
542947117
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-09
Public Version
1
Public Version Date
2024-01-17
Public Version Status
New
Public Device Record Key
a275d158-d0ac-425d-bc7d-8980d55969f1

Device Description

Disposable Ligation Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
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
MND Ligator, Esophageal

GMDN Terms

Code Name
38719 Polypectomy endoscopic ligator, single-use

Identifiers

Type ID
Primary 06934415023337

Customer Contacts