FDA UDI Not in Commercial Distribution 🇺🇸 United States

TEMNO

DI: 10885403087516 · Model: ACT2211 · CAREFUSION 2200, INC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TEMNO
Primary DI
10885403087516
Version / Model
ACT2211
Catalog Number
ACT2211
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-09
Public Version
3
Public Version Date
2023-10-11
Public Version Status
Update
Public Device Record Key
345b2b39-8100-4f7a-bd72-efe602779c82
Distribution End Date
2019-11-30

Device Description

TEMNO NEEDLE BIOPSY 22GX11CM ADJUSTABLE COAXIAL

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
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
FCG Biopsy needle
GDF GUIDE, NEEDLE, SURGICAL

GMDN Terms

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

Identifiers

Type ID
Package 50885403087514
Primary 10885403087516

Customer Contacts

Device Sizes

Type Value Unit Text
Length 11 Centimeter
Needle Gauge 22 Gauge