FDA UDI In Commercial Distribution 🇺🇸 United States

Universal Dilator

DI: M7405210001 · Model: 52-02-01 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Universal Dilator
Primary DI
M7405210001
Version / Model
52-02-01
Catalog Number
521-0001
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-19
Public Version
1
Public Version Date
2023-12-27
Public Version Status
New
Public Device Record Key
e0dd2784-5a81-40fa-b95b-0c0d5c6c18af

Device Description

Pedicle Marker Inserter

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
MR Unsafe
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
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary M7405210001

Customer Contacts

Phone
651-256-8500