FDA UDI In Commercial Distribution 🇺🇸 United States

Stryker

DI: B504AE2793511030 · Model: 279-351-103 · Provision
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stryker
Primary DI
B504AE2793511030
Version / Model
279-351-103
Company Name
Provision
Labeler DUNS
016889401
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-08
Public Version
1
Public Version Date
2021-03-16
Public Version Status
New
Public Device Record Key
3c0c89a9-4ed8-475a-b926-ece5369e1017

Device Characteristics

Single Use
Yes
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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

GMDN Terms

Code Name
61817 Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed

Identifiers

Type ID
Primary B504AE2793511030

Customer Contacts

Phone
541-422-8880

Premarket Submissions

Submission Number Supplement Number
K173740 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
7 – 32 Degrees Celsius