FDA UDI Not in Commercial Distribution 🇺🇸 United States

ETHICON

DI: 10705031005082 · Model: 3909 · ETHICON INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ETHICON
Primary DI
10705031005082
Version / Model
3909
Catalog Number
3909
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
6
Public Version Date
2023-03-16
Public Version Status
Update
Public Device Record Key
20aedfb2-57bd-474c-bef2-1ced789bf9a3
Distribution End Date
2023-03-15

Device Description

Flexible Tip Applicator

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
52751 Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use

Identifiers

Type ID
Package 20705031005089
Primary 10705031005082
Package 30705031005086

Customer Contacts