FDA UDI In Commercial Distribution 🇺🇸 United States

Glucertain

DI: 00850031608115 · Model: 30228 · CELLERA LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Glucertain
Primary DI
00850031608115
Version / Model
30228
Catalog Number
30228
Company Name
CELLERA LLC
Labeler DUNS
960091929
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-08
Public Version
1
Public Version Date
2023-06-16
Public Version Status
New
Public Device Record Key
a641c917-2a78-4799-9bc2-f0a127dde5e8

Device Description

Safety Lancet, 28 ga., 100/box, 10 boxes/case

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
Yes
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
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 00850031608122
Primary 00850031608115
Package 10850031608129

Customer Contacts

Phone
800-892-2391