FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277332690 · Model: MDS52232045 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10888277332690
Version / Model
MDS52232045
Catalog Number
MDS52232045
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
4
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
22d9d2e0-7e56-4550-9606-475f8f7e14a6

Device Description

LAP, SUCTION, COAGULATOR, "L" TIP, 45CM

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
HFI COAGULATOR, CULDOSCOPIC (AND ACCESSORIES)

GMDN Terms

Code Name
35524 Flexible endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 10888277332690

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K925114 000