FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10724995191242 · Model: BF001 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
NA
Primary DI
10724995191242
Version / Model
BF001
Catalog Number
BF001
Company Name
STERIS CORPORATION
Labeler DUNS
036985604
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2021-04-23
Public Version
1
Public Version Date
2021-05-03
Public Version Status
New
Public Device Record Key
b5d769c3-861c-4c62-b86c-003217390944

Device Description

The OT1000 Traction Boot Foam Pads with Straps secure to patients feet with straps.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HST Apparatus, traction, non-powered

GMDN Terms

Code Name
46509 Traction boot

Identifiers

Type ID
Unit of Use 00724995191245
Primary 10724995191242

Customer Contacts