FDA UDI Not in Commercial Distribution 🇺🇸 United States

MAXI-DRIVER

DI: 20845854009922 · Model: L130 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MAXI-DRIVER
Primary DI
20845854009922
Version / Model
L130
Catalog Number
L130
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-13
Public Version
2
Public Version Date
2024-06-10
Public Version Status
Update
Public Device Record Key
6a2fa994-9ac2-42a9-82e1-756c9fe1b24c
Distribution End Date
2024-06-07

Device Description

MAXI-DRIVER Blade, Oscillating, Coarse, 0.97x73.5x29.3mm

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
Primary 20845854009922

Customer Contacts