FDA UDI In Commercial Distribution 🇺🇸 United States

Omnicurve

DI: 07613327554649 · Model: 1032-130-000 · STRYKER CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Omnicurve
Primary DI
07613327554649
Version / Model
1032-130-000
Catalog Number
1032-130-000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-02
Public Version
1
Public Version Date
2023-11-10
Public Version Status
New
Public Device Record Key
303462a1-a7c9-4233-af37-f881a54fa5cd

Device Description

11G 30mm Fracture Kit

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
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
NDN CEMENT, BONE, VERTEBROPLASTY
HRX Arthroscope

GMDN Terms

Code Name
47129 Balloon kyphoplasty kit

Identifiers

Type ID
Primary 07613327554649

Customer Contacts

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
10 – 60 Percent (%) Relative Humidity
Type
Storage Environment Humidity
Temperature Range
10 – 60 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
12 – 25 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
12 – 25 Degrees Celsius