FDA UDI In Commercial Distribution 🇺🇸 United States

REFLEX

DI: 20653405037016 · Model: 8735 · Conmed Corporation
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
6

Basic Information

Brand Name
REFLEX
Primary DI
20653405037016
Version / Model
8735
Catalog Number
8735
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2020-11-13
Public Version
3
Public Version Date
2022-07-18
Public Version Status
Update
Public Device Record Key
c8ab917e-ec34-4c45-aaf4-0e6236c82ac8

Device Description

Reflex TL, Skin Stapler with tissue lift, 35 wide

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
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FZQ CLIP, REMOVABLE (SKIN)
QQS Stapler, skin

GMDN Terms

Code Name
35884 Skin stapler/staple, non-bioabsorbable

Identifiers

Type ID
Package 10653405037019
Primary 20653405037016
Unit of Use 00653405037012

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
10 – 32 Degrees Celsius