FDA UDI In Commercial Distribution 🇺🇸 United States

Litetouch

DI: 00840216124332 · Model: 203TC · Asp Global, LLC
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Litetouch
Primary DI
00840216124332
Version / Model
203TC
Company Name
Asp Global, LLC
Labeler DUNS
080361159
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-16
Public Version
1
Public Version Date
2023-11-24
Public Version Status
New
Public Device Record Key
9478c5a5-bcef-4197-964e-585abed9d411

Device Description

LITE TOUCH MICRO THIN LANCETS - 33G - 1/EA, 100EA/BX, 100BX/CS (10000EA)

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
No
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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature
QRL Multiple Use Blood Lancet For Single Patient Use Only

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable

Identifiers

Type ID
Primary 00840216124332
Package 00840216124349
Package 10840216124339