FDA UDI In Commercial Distribution 🇺🇸 United States

Synergetics

DI: 10841305111414 · Model: SE5623 · SYNERGETICS USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Synergetics
Primary DI
10841305111414
Version / Model
SE5623
Catalog Number
SE5623
Company Name
SYNERGETICS USA, INC.
Labeler DUNS
021056726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-01
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7faf47e4-9f6a-4843-b386-7b8f82e9948a

Device Description

23ga Stellaris Elite Vitrectomy Probe

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
Yes
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
HQE Instrument, vitreous aspiration and cutting, ac-powered

GMDN Terms

Code Name
59528 Hereditary cerebral haemorrhage with amyloidosis (Dutch type) IVD, kit, nucleic acid technique (NAT)

Identifiers

Type ID
Package 20841305111428
Primary 10841305111414

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit