FDA UDI In Commercial Distribution 🇺🇸 United States

Paradigm

DI: 00850042604205 · Model: 1200017 · Proprio, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Paradigm
Primary DI
00850042604205
Version / Model
1200017
Catalog Number
1200017
Company Name
Proprio, Inc.
Labeler DUNS
010254854
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-21
Public Version
2
Public Version Date
2026-01-13
Public Version Status
Update
Public Device Record Key
db80d259-23a9-4d0e-8cbf-90a90dcd431a

Device Description

Paradigm DRF Mini Clamp

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
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
OLO Orthopedic Stereotaxic Instrument

GMDN Terms

Code Name
46751 Bone holding forceps
61407 Surgical optical-tracking spatial marker, reusable

Identifiers

Type ID
Primary 00850042604205

Customer Contacts

Phone
206-848-6303

Premarket Submissions

Submission Number Supplement Number
K243258 000
K250879 000
K252950 000