FDA UDI Not in Commercial Distribution 🇺🇸 United States

NETCELL

DI: 05060165010042 · Model: 10-105 · NETWORK MEDICAL PRODUCTS LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
NETCELL
Primary DI
05060165010042
Version / Model
10-105
Company Name
NETWORK MEDICAL PRODUCTS LIMITED
Labeler DUNS
458670304
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2019-08-05
Public Version
4
Public Version Date
2024-10-09
Public Version Status
Update
Public Device Record Key
7b68f8c8-a415-48f1-b3dd-cab78f1ea7f1
Distribution End Date
2024-10-08

Device Description

NETCELL 6.0 Nasal

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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
LYA Splint, Intranasal Septal

GMDN Terms

Code Name
31919 Intranasal splint, non-biodegradable

Identifiers

Type ID
Primary 05060165010042
Unit of Use 05056100703087