FDA UDI In Commercial Distribution 🇺🇸 United States

Synergetics

DI: 20841305107261 · Model: 56.20.23P · SYNERGETICS USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

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Basic Information

Brand Name
Synergetics
Primary DI
20841305107261
Version / Model
56.20.23P
Catalog Number
56.20.23P
Company Name
SYNERGETICS USA, INC.
Labeler DUNS
021056726
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2016-08-26
Public Version
5
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
980a865f-c68c-4173-8e4d-de99a1f7abb3

Device Description

23ga Vivid™ Endo Illuminator

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MPA Endoilluminator

GMDN Terms

Code Name
45193 Ophthalmic fibreoptic light instrument, single-use

Identifiers

Type ID
Primary 20841305107261
Unit of Use 10841305100784

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit