FDA UDI In Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403240881 · Model: LA103-RLL · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
V. Mueller
Primary DI
10885403240881
Version / Model
LA103-RLL
Catalog Number
LA103-RLL
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-30
Public Version
4
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
f8204492-90c7-48f0-a937-c0bbc0dddbc8

Device Description

V. Mueller HIGH FLOW INSUFFLATION TUBING WITH ROTATING LUER LOCK, .3 MICRON FILTER, 10 FT. 20 EACH/BOX

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
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKC Tubing/tubing with filter, insufflation, laparoscopic

GMDN Terms

Code Name
60738 Endoscopic insufflation tubing set, single-use

Identifiers

Type ID
Package 20885403240888
Primary 10885403240881

Customer Contacts