FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780537311 · Model: INS030 · INTEGRA PAIN MANAGEMENT
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Integra®
Primary DI
10381780537311
Version / Model
INS030
Catalog Number
INS030
Company Name
INTEGRA PAIN MANAGEMENT
Labeler DUNS
030370299
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-19
Public Version
1
Public Version Date
2024-11-27
Public Version Status
New
Public Device Record Key
c970f16a-a12c-4a45-b68a-0765ac9e9915

Device Description

Integra® Hand Drill - Sterile

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HBG DRILLS, BURRS, TREPHINES & ACCESSORIES (MANUAL)

GMDN Terms

Code Name
46281 Manual cranial rotary handpiece, single-use

Identifiers

Type ID
Previous 10381780263890
Primary 10381780537311

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K961113 000