FDA UDI In Commercial Distribution 🇺🇸 United States

Synergetics

DI: 10841305100692 · Model: 56.02P · SYNERGETICS USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Synergetics
Primary DI
10841305100692
Version / Model
56.02P
Catalog Number
56.02P
Company Name
SYNERGETICS USA, INC.
Labeler DUNS
021056726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-15
Public Version
1
Public Version Date
2020-06-23
Public Version Status
New
Public Device Record Key
6747c7c0-5260-4275-bb66-2f6b0fc3e7a0

Device Description

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
No
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 10841305100692
Package 20841305107179

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit