FDA UDI In Commercial Distribution 🇺🇸 United States

Synergetics

DI: 10841305102634 · Model: 52.00 · SYNERGETICS USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Synergetics
Primary DI
10841305102634
Version / Model
52.00
Catalog Number
52.00
Company Name
SYNERGETICS USA, INC.
Labeler DUNS
021056726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-18
Public Version
1
Public Version Date
2020-09-28
Public Version Status
New
Public Device Record Key
516fed7d-8de9-4fb6-87b9-269f946b30c8

Device Description

Branch Retinal Vein Occlusion (BRVO) Knife

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
Yes
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
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
62478 Ophthalmic soft-tissue manipulation forceps, probe-like, single-use

Identifiers

Type ID
Package 20841305109111
Primary 10841305102634

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit