FDA UDI In Commercial Distribution 🇺🇸 United States

De Soutter Medical

DI: 05051471189478 · Model: 20320 · DE SOUTTER MEDICAL LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
De Soutter Medical
Primary DI
05051471189478
Version / Model
20320
Catalog Number
20320
Company Name
DE SOUTTER MEDICAL LIMITED
Labeler DUNS
458064144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-28
Public Version
1
Public Version Date
2022-12-06
Public Version Status
New
Public Device Record Key
b1e91ea4-0edd-4f4a-8541-da4925b6342a

Device Description

LQ-922 PULSE LAVAGE ATTACHMENT - AESCULAP 3Ti DRIVE

Device Characteristics

Single Use
No
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
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
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
GEY Motor, Surgical Instrument, Ac-Powered

GMDN Terms

Code Name
47845 Surgical power tool adaptor

Identifiers

Type ID
Primary 05051471189478