FDA UDI In Commercial Distribution 🇺🇸 United States

Rasp

DI: 03760418040209 · Model: 57.003.00T · SC MEDICA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rasp
Primary DI
03760418040209
Version / Model
57.003.00T
Company Name
SC MEDICA
Labeler DUNS
267135902
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-13
Public Version
1
Public Version Date
2024-11-21
Public Version Status
New
Public Device Record Key
e167917a-ee37-473c-b63b-3845e01ef1c3

Device Description

Rasp with titanium handle

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
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
12844 Orthopaedic osteotome

Identifiers

Type ID
Primary 03760418040209