FDA UDI In Commercial Distribution 🇺🇸 United States

xinle

DI: 06950383616319 · Model: XL-E 28G · Hebei Xinle Sci&Tech Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

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Basic Information

Brand Name
xinle
Primary DI
06950383616319
Version / Model
XL-E 28G
Catalog Number
XLE2822
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
2
Public Version Date
2024-11-11
Public Version Status
Update
Public Device Record Key
81b711fc-ec72-4e41-b4e3-0b679a16ec11

Device Description

LANCET PURPLE 28G X 2.2MM

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 16950383616316
Primary 06950383616319
Unit of Use 86950383616315

Device Sizes

Type Value Unit Text
Needle Gauge 28 Gauge

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature