FDA UDI In Commercial Distribution 🇺🇸 United States

ORLocate

DI: 00724995243678 · Model: ORLocate Roll Stand · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
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
ORLocate
Primary DI
00724995243678
Version / Model
ORLocate Roll Stand
Catalog Number
ORL100160
Company Name
STERIS CORPORATION
Labeler DUNS
036985604
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-17
Public Version
1
Public Version Date
2025-04-25
Public Version Status
New
Public Device Record Key
aee76144-47be-4d39-b0dc-db3f78e16f95

Device Description

The ORLocate Roll Stand is part of the ORLocate Sponge System.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LWH Counter, sponge, surgical

GMDN Terms

Code Name
63219 Radio-frequency identification reader

Identifiers

Type ID
Primary 00724995243678
Previous 00724995221683

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K100551 000