FDA UDI In Commercial Distribution 🇺🇸 United States

LANZA

DI: 20845854649159 · Model: 9391M · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
6

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Basic Information

Brand Name
LANZA
Primary DI
20845854649159
Version / Model
9391M
Catalog Number
9391M
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2020-12-23
Public Version
5
Public Version Date
2024-08-02
Public Version Status
Update
Public Device Record Key
15b6483a-5c54-4c7a-9661-a80ca2b8430b

Device Description

15° LANZA, 4.2 MM X 13 CM

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
41499 Arthroscopic shaver system blade, single-use

Identifiers

Type ID
Package 30845854649156
Primary 20845854649159
Unit of Use 00845854649155
Previous 10845854850404

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 15 degree

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry