FDA UDI In Commercial Distribution 🇺🇸 United States

ETHICON SECURESTRAP

DI: 10705031231054 · Model: OPSTRAP20 · ETHICON, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ETHICON SECURESTRAP
Primary DI
10705031231054
Version / Model
OPSTRAP20
Catalog Number
OPSTRAP20, OPSTRAP20R
Company Name
ETHICON, LLC
Labeler DUNS
079402290
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-23
Public Version
6
Public Version Date
2022-01-18
Public Version Status
Update
Public Device Record Key
cb4003b9-82d0-427b-8077-4f55c8f25411

Device Description

ETHICON SECURESTRAP ABSORBABLE FIXATION DEVICE

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
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
GDW STAPLE, IMPLANTABLE

GMDN Terms

Code Name
59873 Open-surgery manual linear stapler, single-use

Identifiers

Type ID
Package 30705031231058
Primary 10705031231054

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123114 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 30 Degrees Celsius