FDA UDI Not in Commercial Distribution 🇺🇸 United States

E-PACK

DI: 20705031241906 · Model: 9844E · ETHICON INC.
Product Codes
7
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
E-PACK
Primary DI
20705031241906
Version / Model
9844E
Catalog Number
9844E
Company Name
ETHICON INC.
Labeler DUNS
002144145
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-29
Public Version
7
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
15bf84b4-eaf3-4023-850f-7228b3088c7b
Distribution End Date
2019-08-19

Device Description

E-Pack Procedure Kit

Device Characteristics

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

GMDN Terms

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

Identifiers

Type ID
Package 30705031241903
Primary 20705031241906

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is opened or damaged