FDA UDI In Commercial Distribution 🇺🇸 United States

Synergetics

DI: 10841305101231 · Model: 16579 · SYNERGETICS USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Synergetics
Primary DI
10841305101231
Version / Model
16579
Catalog Number
16579
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
a1e8736b-a528-4a37-bcc7-8f9995c8892d

Device Description

Three-Way Infusion Tubing Set

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 20841305107711
Primary 10841305101231

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit