FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277416178 · Model: ONBFCA12SR · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10888277416178
Version / Model
ONBFCA12SR
Catalog Number
ONBFCA12SR
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
df65f577-278d-471b-b5bf-c90087555dc4

Device Description

ONBFCA12ST @VERSAPORT V2 OPT BLADELESS 1

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 20888277416175
Primary 10888277416178

Customer Contacts