FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED

DI: 10845854029602 · Model: H9002 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
6

Basic Information

Brand Name
CONMED
Primary DI
10845854029602
Version / Model
H9002
Catalog Number
H9002
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2021-10-14
Public Version
4
Public Version Date
2023-05-04
Public Version Status
Update
Public Device Record Key
84858bd2-7640-42bd-9347-9e3c6d0e37ad

Device Description

4.0MM OR 4.5MM BUR SHEATH TO MAKE UNHOODED BUR

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
GFF BUR, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
41499 Arthroscopic shaver system blade, single-use

Identifiers

Type ID
Package 20845854029609
Primary 10845854029602
Unit of Use 00845854029605

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY