FDA UDI In Commercial Distribution 🇺🇸 United States

LANDANGER

DI: 03661219343776 · Model: H210002 · LANDANGER
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LANDANGER
Primary DI
03661219343776
Version / Model
H210002
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
200f69c1-0a03-4da2-a64e-451be29f22fb

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
FZS Curette, Surgical, General Use

GMDN Terms

Code Name
11290 Open-surgery dissector

Identifiers

Type ID
Primary 03661219343776