FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613252027232 · Model: 5450850001 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
07613252027232
Version / Model
5450850001
Catalog Number
5450850001
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-15
Public Version
3
Public Version Date
2024-01-01
Public Version Status
Update
Public Device Record Key
99a174b6-2796-4a4a-a343-b12869e3455b
Distribution End Date
2024-01-01

Device Description

Reusable Suction Canister

Device Characteristics

Single Use
No
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
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KDQ BOTTLE, COLLECTION, VACUUM

GMDN Terms

Code Name
44778 Soft-tissue ultrasonic surgical system

Identifiers

Type ID
Primary 07613252027232

Customer Contacts