FDA UDI Not in Commercial Distribution 🇺🇸 United States

REFLEX

DI: 10653405034919 · Model: 16050 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REFLEX
Primary DI
10653405034919
Version / Model
16050
Catalog Number
16050
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
7
Public Version Date
2024-02-02
Public Version Status
Update
Public Device Record Key
842e491d-d27c-4d4b-8e48-0138848e0007
Distribution End Date
2024-02-01

Device Description

REFLEX STR BLADED/SHIELDED SURGICAL TROCAR 5MM

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
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
42412 Laparoscopic access cannula, single-use

Identifiers

Type ID
Primary 10653405034919

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K924761 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Bladed/Shielded Surgical Trocar

Storage Conditions

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