FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780261841 · Model: 3404696 · INTEGRA PAIN MANAGEMENT
Product Codes
0
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780261841
Version / Model
3404696
Company Name
INTEGRA PAIN MANAGEMENT
Labeler DUNS
030370299
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-30
Public Version
3
Public Version Date
2019-12-12
Public Version Status
Update
Public Device Record Key
1d41d407-05de-4efe-baca-9da8e4f71144

Device Description

NERVE BLOCK 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
59012 Peripheral nerve-block blunt needle access cannula

Identifiers

Type ID
Package 30381780261845
Primary 10381780261841
Secondary M61034046961

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Storage Environment Temperature: 15 C to 30 C (59 F to 86 F)