FDA UDI In Commercial Distribution 🇺🇸 United States

KetoBM

DI: 00860001641738 · Model: KBM-L1 · Ketobm LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KetoBM
Primary DI
00860001641738
Version / Model
KBM-L1
Company Name
Ketobm LLC
Labeler DUNS
118745029
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-21
Public Version
1
Public Version Date
2022-11-29
Public Version Status
New
Public Device Record Key
f11508fd-8c7f-45ac-98bc-51a2e46bef60

Device Description

Lancets - Box of 100

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

GMDN Terms

Code Name
61579 Blood lancet, single-use

Identifiers

Type ID
Primary 00860001641738

Customer Contacts

Phone
307-228-1744