FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780262152 · Model: 3404866 · INTEGRA PAIN MANAGEMENT
Product Codes
0
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Integra®
Primary DI
10381780262152
Version / Model
3404866
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
4
Public Version Date
2024-04-05
Public Version Status
Update
Public Device Record Key
2b12d203-9a6a-45d3-8e41-3e8922026fe3
Distribution End Date
2023-12-04

Device Description

UNIVERSAL 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 30381780262156
Primary 10381780262152
Secondary M61034048661

Customer Contacts

Storage Conditions

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