FDA UDI In Commercial Distribution 🇺🇸 United States

Broadway System

DI: 07613327639032 · Model: BRW8E100D-3PK01 · Stryker Corporation
Product Codes
0
GMDN Terms
3
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
Broadway System
Primary DI
07613327639032
Version / Model
BRW8E100D-3PK01
Catalog Number
BRW8E100D-3PK01
Company Name
Stryker Corporation
Labeler DUNS
042405446
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-12
Public Version
1
Public Version Date
2025-03-20
Public Version Status
New
Public Device Record Key
dcdc9037-e571-478f-9b25-b3793657d9d0

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use
38128 Vascular dilator, single-use
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Primary 07613327639032

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry, dark place.