FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10884389179642 · Model: END7754089CR · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10884389179642
Version / Model
END7754089CR
Catalog Number
END7754089CR
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-14
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
54c6a517-194b-4a31-b072-1c1bb6dec9f0

Device Description

ENDO CLINCH, ATRAUMATIC, SERRATED, C

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
35524 Flexible endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 10884389179642

Customer Contacts