FDA UDI In Commercial Distribution 🇺🇸 United States

Orthopedic manual surgical instrument

DI: 04719883337245 · Model: 420-0408C · BAUI BIOTECH CO. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Orthopedic manual surgical instrument
Primary DI
04719883337245
Version / Model
420-0408C
Company Name
BAUI BIOTECH CO. LTD.
Labeler DUNS
656775504
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-14
Public Version
1
Public Version Date
2025-01-22
Public Version Status
New
Public Device Record Key
e0c66da0-8b9c-4aaa-9726-2169b35a1228

Device Description

8mm Trial

Device Characteristics

Single Use
Yes
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
Yes
Has Expiration Date
Yes
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
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 04719883337245