FDA UDI In Commercial Distribution 🇺🇸 United States

RELION

DI: 00365702702660 · Model: 09556672001 · Roche Diagnostics Operations, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RELION
Primary DI
00365702702660
Version / Model
09556672001
Catalog Number
09556672001
Company Name
Roche Diagnostics Operations, Inc.
Labeler DUNS
141608724
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-19
Public Version
1
Public Version Date
2022-10-27
Public Version Status
New
Public Device Record Key
8beb33b5-9f67-4ddc-a7e9-6ba0d4dfb4b4

Device Description

Relion Platinum Lancing Device

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QRL Multiple Use Blood Lancet For Single Patient Use Only

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable
45142 Blood lancing device tip

Identifiers

Type ID
Primary 00365702702660