FDA UDI In Commercial Distribution 🇺🇸 United States

LANDANGER

DI: 03661219339298 · Model: C100581 · LANDANGER
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LANDANGER
Primary DI
03661219339298
Version / Model
C100581
Company Name
LANDANGER
Labeler DUNS
299889175
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-23
Public Version
1
Public Version Date
2022-10-03
Public Version Status
New
Public Device Record Key
49214d3f-62a2-455c-b9fa-ea3afb865893

Device Characteristics

Single Use
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
DWS Instruments, Surgical, Cardiovascular

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 03661219339298