FDA UDI In Commercial Distribution 🇺🇸 United States

uNion MAX

DI: 00810076334868 · Model: UU201-21-4024 · Ulrich Medical Usa, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
uNion MAX
Primary DI
00810076334868
Version / Model
UU201-21-4024
Company Name
Ulrich Medical Usa, Inc.
Labeler DUNS
624083866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-05
Public Version
2
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
f647d330-2f05-476e-97b7-1b44e120de10

Device Description

Screw, Ø4.0 x 24mm, Self-Drilling Bronze, Variable

Device Characteristics

Single Use
Yes
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
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00810076334868

Customer Contacts

Phone
636-519-0268

Premarket Submissions

Submission Number Supplement Number
K240515 000