FDA UDI Not in Commercial Distribution 🇺🇸 United States

Temno

DI: 10885403089985 · Model: PP1710 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Temno
Primary DI
10885403089985
Version / Model
PP1710
Catalog Number
PP1710
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-18
Public Version
2
Public Version Date
2023-10-12
Public Version Status
Update
Public Device Record Key
171752f3-fb6c-4135-8a76-73ccd2039a93
Distribution End Date
2019-11-30

Device Description

Temno Coaxial Introducer Needle 17G X10CM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GDF GUIDE, NEEDLE, SURGICAL

GMDN Terms

Code Name
16835 Soft-tissue biopsy procedure kit, non-medicated

Identifiers

Type ID
Package 50885403089983
Primary 10885403089985

Customer Contacts