FDA UDI In Commercial Distribution 🇺🇸 United States

Integra

DI: 10381780178453 · Model: 31233 · INTEGRA PAIN MANAGEMENT
Product Codes
0
GMDN Terms
3
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra
Primary DI
10381780178453
Version / Model
31233
Company Name
INTEGRA PAIN MANAGEMENT
Labeler DUNS
030370299
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-29
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d958516b-1c4c-4f7a-8fa4-431b1fc7c64f

Device Description

ACCUDRAIN WITHOUT ANTI REFLUX, HERMETIC LARGE STYLE CATHETER, AND CRANIAL ACCESS KIT

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
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
61797 Lumbar cerebrospinal fluid drainage catheterization kit
61798 Ventricular cerebrospinal fluid drainage catheterization kit
46281 Manual cranial rotary handpiece, single-use

Identifiers

Type ID
Secondary M610312331
Primary 10381780178453

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
68 – 77 Degrees Fahrenheit