FDA UDI In Commercial Distribution 🇺🇸 United States

LANDANGER

DI: 03661219000839 · Model: A30075 · LANDANGER
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LANDANGER
Primary DI
03661219000839
Version / Model
A30075
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
2
Public Version Date
2023-01-10
Public Version Status
Update
Public Device Record Key
96f4f3e9-5fe0-4d3e-90e3-f46dede3e0da

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
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
62468 Surgical soft-tissue manipulation forceps, scissors-like, reusable

Identifiers

Type ID
Primary 03661219000839