FDA UDI In Commercial Distribution 🇺🇸 United States

INTREX

DI: 10845854010990 · Model: 00507132300 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
INTREX
Primary DI
10845854010990
Version / Model
00507132300
Catalog Number
5071-323
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-09-24
Public Version
3
Public Version Date
2023-05-26
Public Version Status
Update
Public Device Record Key
a3d5c35b-6c93-47ef-b8cb-9dbfdf1b2bfe

Device Description

INTREX LARGE BONE OSCILLATING SAW BLADE 25.0 X 90.0 X 1.19MM

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GFA BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

GMDN Terms

Code Name
46476 Surgical saw blade, oscillating, single-use

Identifiers

Type ID
Package 20845854010997
Primary 10845854010990
Unit of Use 00845854010993

Customer Contacts

Device Sizes

Type Value Unit Text
Width 25 Millimeter
Length 90 Millimeter
Height 1.19 Millimeter