FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10845854023631 · Model: 00505903201 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
NA
Primary DI
10845854023631
Version / Model
00505903201
Catalog Number
5059-032-01
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2021-10-06
Public Version
2
Public Version Date
2023-05-25
Public Version Status
Update
Public Device Record Key
06cd7f6d-ace1-409f-9223-ca8043d1360b

Device Description

STERNUM SAW BLADE NON-STERILE BULK PACK (5 PACKS OF 10)

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
No

Product Codes

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

GMDN Terms

Code Name
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Unit of Use 00845854023634
Primary 10845854023631

Customer Contacts