FDA UDI In Commercial Distribution 🇺🇸 United States

Ziplyft Device

DI: 00860011170600 · Model: PKG-90-OSH-000002 · Osheru, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ziplyft Device
Primary DI
00860011170600
Version / Model
PKG-90-OSH-000002
Company Name
Osheru, L.L.C.
Labeler DUNS
094081018
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-18
Public Version
1
Public Version Date
2023-12-26
Public Version Status
New
Public Device Record Key
0632636d-fd0d-4bb3-8f83-a341d0e79f81

Device Description

Non-Sterile Packaged Ziplyft Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Hydrogen Peroxide

Product Codes

Code Name
HNN Knife, Ophthalmic

GMDN Terms

Code Name
46741 Ophthalmic knife, single-use

Identifiers

Type ID
Primary 00860011170600