FDA UDI Not in Commercial Distribution 🇺🇸 United States

E-PACK

DI: 20705031234601 · Model: 9472E · ETHICON INC.
Product Codes
7
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
E-PACK
Primary DI
20705031234601
Version / Model
9472E
Catalog Number
9472E
Company Name
ETHICON INC.
Labeler DUNS
002144145
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-20
Public Version
6
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
ee0d0bc7-8292-4dd7-ba78-bbb6ea13af86
Distribution End Date
2019-07-08

Device Description

E-Pack Procedure Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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
GAM SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID
GAN SUTURE, ABSORBABLE, SYNTHETIC
FZP CLIP, IMPLANTABLE
FTL Mesh, surgical, polymeric
GAQ Suture, nonabsorbable, steel, monofilament and multifilament, sterile
GAW SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE
LDF ELECTRODE, PACEMAKER, TEMPORARY

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 30705031234608
Primary 20705031234601

Customer Contacts