FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 07613327375817 · Model: LF1737 · STRYKER SUSTAINABILITY SOLUTIONS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
07613327375817
Version / Model
LF1737
Catalog Number
LF1737
Company Name
STRYKER SUSTAINABILITY SOLUTIONS, INC.
Labeler DUNS
020198912
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-23
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
88933060-2f1c-4458-b0bc-109b3e2bdf7c

Device Description

Maryland Jaw Sealer/Divider

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
NUJ ELECTROSURGICAL, CUTTING & COAGULATION ACCESSORIES, LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED

GMDN Terms

Code Name
61818 Open-surgery electrosurgical handpiece/electrode, bipolar, reprocessed

Identifiers

Type ID
Package 57613327375812
Primary 07613327375817

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180499 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 5.0 Millimeter
Length 37.0 Centimeter

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-18 – 60 Degrees Celsius