FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 30845854061439 · Model: 57525685 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
30845854061439
Version / Model
57525685
Catalog Number
57525685
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-08-06
Public Version
4
Public Version Date
2023-06-05
Public Version Status
Update
Public Device Record Key
ba6e73e6-7632-409d-aad8-462ad313cea6

Device Description

Fluid trap (10 pieces)

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KDQ BOTTLE, COLLECTION, VACUUM

GMDN Terms

Code Name
44979 Surgical plume evacuation system filter

Identifiers

Type ID
Primary 30845854061439
Unit of Use 00845854061438

Customer Contacts