FDA UDI In Commercial Distribution 🇺🇸 United States

KHEIRON

DI: 03701313002121 · Model: 01BS3010 · S.M.A.I.O
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KHEIRON
Primary DI
03701313002121
Version / Model
01BS3010
Catalog Number
01BS3010
Company Name
S.M.A.I.O
Labeler DUNS
260585710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-18
Public Version
1
Public Version Date
2020-12-28
Public Version Status
New
Public Device Record Key
f80943c9-18af-4d4a-803e-59d1752d5e29

Device Description

Right Ø5.5 rod sagittal bender

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
HXW Bender

GMDN Terms

Code Name
44795 Manual orthopaedic bender, reusable

Identifiers

Type ID
Primary 03701313002121

Customer Contacts

Phone
+33469842302