FDA UDI In Commercial Distribution 🇺🇸 United States

xinle

DI: 06950383616210 · Model: XL-B 30G · Hebei Xinle Sci&Tech Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
xinle
Primary DI
06950383616210
Version / Model
XL-B 30G
Catalog Number
XLB3018
Company Name
Hebei Xinle Sci&Tech Co., Ltd.
Labeler DUNS
529813593
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-09-14
Public Version
1
Public Version Date
2023-09-22
Public Version Status
New
Public Device Record Key
916d7f32-e793-4664-a1d0-8561b93c1bdd

Device Description

LANCET GRAY 30G X 1.8MM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 16950383616217
Primary 06950383616210
Unit of Use 86950383616216

Premarket Submissions

Submission Number Supplement Number
K221839 000

Device Sizes

Type Value Unit Text
Needle Gauge 30 Gauge

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature