FDA UDI In Commercial Distribution 🇺🇸 United States

NaviCam Tether

DI: 00850015518287 · Model: CEE-1 · ANX ROBOTICA CORP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NaviCam Tether
Primary DI
00850015518287
Version / Model
CEE-1
Catalog Number
ES-US-3002
Company Name
ANX ROBOTICA CORP
Labeler DUNS
024972857
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-05
Public Version
1
Public Version Date
2023-01-13
Public Version Status
New
Public Device Record Key
faef845e-bdbf-43a2-b9f9-20bfbf8661a2

Device Description

Tether Accessory. The NaviCam Capsule and NaviCam Tether are disposable sterile products, which serve as an accessory to the NaviCam System to allow for examination of the esophagus prior to releasing the NaviCam Capsule into the stomach. The NaviCam Tether is comprised of a tube which on one end is attached to a capsule cradle and on the other end is attached to a syringe connector. The capsule cradle holds the capsule in place while examining the esophagus. The tube is used to control the downward speed of the capsule in the esophagus. The syringe connector serves for releasing the capsule by attaching to it a standard syringe filled with air. 2 NaviCam Stomach Capsule and NaviCam Tether. After the examination of the esophagus is accomplished, the syringe piston is pushed to release the capsule for examining the stomach with the NaviCam System.

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QKZ Magnetically Maneuvered Capsule Endoscopy System

GMDN Terms

Code Name
38068 Video capsule endoscopy system capsule

Identifiers

Type ID
Primary 00850015518287
Package 10850015518284

Customer Contacts

Phone
770-480-2911

Premarket Submissions

Submission Number Supplement Number
K221608 000