FDA UDI In Commercial Distribution 🇺🇸 United States

neoWave LS

DI: 00818345023932 · Model: 23-K01-0210 · Ht Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
neoWave LS
Primary DI
00818345023932
Version / Model
23-K01-0210
Catalog Number
N/A
Company Name
Ht Medical, LLC
Labeler DUNS
080386764
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-30
Public Version
3
Public Version Date
2023-11-16
Public Version Status
Update
Public Device Record Key
eec47a90-eccf-4459-849f-c4cd7b9c60f6

Device Description

PADDLE SPREADER, 10MM

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
Yes
PM Exempt
No
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Primary 00818345023932

Customer Contacts

Phone
888-594-8633

Premarket Submissions

Submission Number Supplement Number
K182210 000
K222988 000