FDA UDI In Commercial Distribution 🇺🇸 United States

Apollo Revise NXT System

DI: 00811955020940 · Model: APL-REV-NXT · Apollo Endosurgery, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Apollo Revise NXT System
Primary DI
00811955020940
Version / Model
APL-REV-NXT
Catalog Number
APL-REV-NXT
Company Name
Apollo Endosurgery, Inc.
Labeler DUNS
625064352
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-16
Public Version
1
Public Version Date
2023-11-24
Public Version Status
New
Public Device Record Key
9b48d038-1cca-42cb-9e0e-bf6b2cdf1c8a

Device Description

Single Channel Endobariatric 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
MR Conditional
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
QTD Endoscopic Suturing Device For Altering Gastric Anatomy For Weight Loss

GMDN Terms

Code Name
57874 Suturing unit, single-use

Identifiers

Type ID
Primary 00811955020940

Customer Contacts

Phone
855-551-3123