FDA UDI Not in Commercial Distribution 🇺🇸 United States

RFS Instrument

DI: E302RFSCDR359 · Model: RFS-CDR35 · Bioretec Oy
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
RFS Instrument
Primary DI
E302RFSCDR359
Version / Model
RFS-CDR35
Catalog Number
RFS-CDR35
Company Name
Bioretec Oy
Labeler DUNS
368715301
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-23
Public Version
3
Public Version Date
2018-11-22
Public Version Status
Update
Public Device Record Key
43ebd339-a1f1-4c13-b9ed-d0a51e3aa2b5
Distribution End Date
2017-12-31

Device Description

RFS™ Cannulated Drill 3.5

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
32390 Fluted surgical drill bit, reusable

Identifiers

Type ID
Primary E302RFSCDR359

Customer Contacts

Device Sizes

Type Value Unit Text
Width 3.5 Millimeter