FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277416079 · Model: ONB11STFR · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10888277416079
Version / Model
ONB11STFR
Catalog Number
ONB11STFR
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-09
Public Version
1
Public Version Date
2023-10-17
Public Version Status
New
Public Device Record Key
ab0df73b-e28d-4aa0-99f1-609b0fa9082c

Device Description

ONB11STF @VERSAPORT V2 OPT BLADELESS 11

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NLM Laparoscope, general & plastic surgery, reprocessed

GMDN Terms

Code Name
61813 Laparoscopic access cannula, reprocessed

Identifiers

Type ID
Package 20888277416076
Primary 10888277416079

Customer Contacts