FDA UDI In Commercial Distribution 🇺🇸 United States

LUCOOLIFE

DI: 06970240895497 · Model: lucency-T/S/L · Ningbo Luke Medical Devices Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUCOOLIFE
Primary DI
06970240895497
Version / Model
lucency-T/S/L
Company Name
Ningbo Luke Medical Devices Co., Ltd.
Labeler DUNS
541284393
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-27
Public Version
1
Public Version Date
2023-08-04
Public Version Status
New
Public Device Record Key
53fae689-f846-4e23-9b4d-e4368af96cac

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HHE Cup, Menstrual

GMDN Terms

Code Name
47728 Menstrual cup, non-latex, reusable

Identifiers

Type ID
Primary 06970240895497