FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780263135 · Model: CUS1539-07 · INTEGRA PAIN MANAGEMENT
Product Codes
0
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780263135
Version / Model
CUS1539-07
Company Name
INTEGRA PAIN MANAGEMENT
Labeler DUNS
030370299
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
5
Public Version Date
2023-12-05
Public Version Status
Update
Public Device Record Key
1d65e90d-4c2a-47ea-b1db-89a8126b2ac9
Distribution End Date
2019-12-31

Device Description

MEDIAL NERVE BRANCH 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
Yes
Sterilization Prior Use
No

GMDN Terms

Code Name
44057 General surgical procedure kit, medicated

Identifiers

Type ID
Package 30381780263139
Primary 10381780263135
Secondary M610CUS1539071

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)