FDA UDI Not in Commercial Distribution 🇺🇸 United States

E-PACK

DI: 10705031133785 · Model: 9026E · ETHICON INC.
Product Codes
7
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
E-PACK
Primary DI
10705031133785
Version / Model
9026E
Catalog Number
9026E
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
87e5744f-b6e6-497b-8b2f-d4dec59843c1
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
FZP CLIP, IMPLANTABLE
LDF ELECTRODE, PACEMAKER, TEMPORARY
GAW SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE
GAN SUTURE, ABSORBABLE, SYNTHETIC
FTL Mesh, surgical, polymeric
GAQ Suture, nonabsorbable, steel, monofilament and multifilament, sterile

GMDN Terms

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

Identifiers

Type ID
Package 20705031133782
Primary 10705031133785

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 25 Degrees Celsius