FDA UDI In Commercial Distribution 🇺🇸 United States

Spinal instrument

DI: 03700780630950 · Model: 99719001 · CLARIANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spinal instrument
Primary DI
03700780630950
Version / Model
99719001
Company Name
CLARIANCE
Labeler DUNS
296568400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-15
Public Version
1
Public Version Date
2022-03-23
Public Version Status
New
Public Device Record Key
f44e92e1-c89a-4bfc-9d7b-a7b482b33ece

Device Description

HEXAGONAL WRENCH

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 03700780630950

Customer Contacts

Phone
+17738687041