FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277400764 · Model: OR352S · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
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
Medline
Primary DI
10888277400764
Version / Model
OR352S
Catalog Number
OR352S
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-05
Public Version
2
Public Version Date
2025-07-02
Public Version Status
Update
Public Device Record Key
83a156e8-6f77-428f-84fc-b0d6651a3673

Device Description

CONNECTOR,T,STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GAZ TUBING, NONINVASIVE

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Package 20888277400761
Package 30888277400768
Primary 10888277400764

Customer Contacts