FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780264804 · Model: SP0098 · INTEGRA PAIN MANAGEMENT
Product Codes
0
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780264804
Version / Model
SP0098
Catalog Number
SP0098
Company Name
INTEGRA PAIN MANAGEMENT
Labeler DUNS
030370299
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2023-04-17
Public Version Status
Update
Public Device Record Key
bece75b2-7019-4312-ac36-ee31c4211539

Device Description

Integra® Cranial Drill Procedure Kit

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
No
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 30381780264808
Primary 10381780264804
Secondary M610SP00981

Customer Contacts

Storage Conditions

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