FDA UDI In Commercial Distribution 🇺🇸 United States

Synergetics

DI: 20841305109593 · Model: 70023SID · SYNERGETICS USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
Synergetics
Primary DI
20841305109593
Version / Model
70023SID
Catalog Number
70023SID
Company Name
SYNERGETICS USA, INC.
Labeler DUNS
021056726
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2016-07-22
Public Version
5
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
a5a8e829-2e40-49d7-8e5d-91b42b192be7

Device Description

23ga VersaVIT 2.0™ Procedure Pack with Illuminated Directional Laser Probe

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
45150 Ophthalmic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 20841305109593
Unit of Use 10841305109589

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit