FDA UDI In Commercial Distribution 🇺🇸 United States

RENOVOLIFE LLC

DI: M734RNL2510040 · Model: RNL251004 · RENOVO LIFE LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RENOVOLIFE LLC
Primary DI
M734RNL2510040
Version / Model
RNL251004
Catalog Number
RNL-251-004
Company Name
RENOVO LIFE LLC
Labeler DUNS
059066475
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-10
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9494f19e-24cd-4910-a3af-f8bace3c7a3d

Device Description

Intramedullary Fixation Rod, 4.5mm

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
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HSB Rod, Fixation, Intramedullary And Accessories

GMDN Terms

Code Name
56645 Tibia nail, non-sterile

Identifiers

Type ID
Primary M734RNL2510040

Customer Contacts