FDA UDI Not in Commercial Distribution 🇺🇸 United States

ETHICON

DI: 10705031147836 · Model: 3920 · ETHICON INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ETHICON
Primary DI
10705031147836
Version / Model
3920
Catalog Number
3920
Company Name
ETHICON INC.
Labeler DUNS
002144145
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-23
Public Version
7
Public Version Date
2023-03-17
Public Version Status
Update
Public Device Record Key
43f9895c-ab13-48d9-a4e8-a30f00251d49
Distribution End Date
2023-03-16

Device Description

Control Tip

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMF Syringe, piston

GMDN Terms

Code Name
64222 Haematological concentrate/haemostatic agent applicator cannula, open-surgery

Identifiers

Type ID
Package 20705031147833
Primary 10705031147836
Package 30705031147830

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 30 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damaged