FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10845854024409 · Model: 21.1002 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10845854024409
Version / Model
21.1002
Catalog Number
21.1002
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
c8941bed-b8fe-4bf2-bd97-236716a0a70a

Device Description

4.0MM X 130MM MAXI-PROBE, STRAIGHT

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
No
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
HXB PROBE

GMDN Terms

Code Name
35948 Endoscopic surgical probe

Identifiers

Type ID
Direct Marking 30845854024403
Primary 10845854024409

Customer Contacts

Device Sizes

Type Value Unit Text
Width 4 Millimeter
Length 130 Millimeter