FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780464952 · Model: 3405317 · INTEGRA PAIN MANAGEMENT
Product Codes
0
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780464952
Version / Model
3405317
Company Name
INTEGRA PAIN MANAGEMENT
Labeler DUNS
030370299
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-07
Public Version
5
Public Version Date
2023-12-05
Public Version Status
Update
Public Device Record Key
cee87401-f75e-44a9-bcb0-6888e51a35f1
Distribution End Date
2019-12-31

Device Description

XCELL PRP (by Apex Biologix)

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
44057 General surgical procedure kit, medicated

Identifiers

Type ID
Primary 10381780464952
Package 30381780464956

Customer Contacts