FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780431954 · Model: 10-560 · INTEGRA PAIN MANAGEMENT
Product Codes
0
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780431954
Version / Model
10-560
Catalog Number
10-560
Company Name
INTEGRA PAIN MANAGEMENT
Labeler DUNS
030370299
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-03
Public Version
4
Public Version Date
2023-04-17
Public Version Status
Update
Public Device Record Key
5e37abf7-c757-4095-bef4-86b8090e1024

Device Description

Integra® Lumbar Prep Tray

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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
No
Sterilization Prior Use
No

GMDN Terms

Code Name
46281 Manual cranial rotary handpiece, single-use

Identifiers

Type ID
Package 30381780431958
Primary 10381780431954
Previous 10381780260356

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do Not Use If Package Is Damaged
Type
Storage Environment Temperature
Temperature Range
68 – 77 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius