FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613154495597 · Model: 0700020000S1 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
07613154495597
Version / Model
0700020000S1
Catalog Number
0700020000S1
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a04446f0-e888-40af-b93c-802182f55940

Device Description

Low Pressure 4-Port Manifold

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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FYD APPARATUS, EXHAUST, SURGICAL

GMDN Terms

Code Name
47998 Surgical fluid/smoke waste management system

Identifiers

Type ID
Package 37613154495598
Primary 07613154495597

Customer Contacts