FDA UDI In Commercial Distribution 🇺🇸 United States

WECK

DI: 24026704600971 · Model: IPN009005 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
WECK
Primary DI
24026704600971
Version / Model
IPN009005
Catalog Number
544124
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-15
Public Version
3
Public Version Date
2020-01-29
Public Version Status
Update
Public Device Record Key
173c8f21-93c0-4974-9a77-a84a46f5053b

Device Description

HEM-O-LOK REMOVER LARGE/EXTRA LARGE 11"

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GDO Applier, surgical, clip

GMDN Terms

Code Name
10895 Surgical clip remover, reusable

Identifiers

Type ID
Primary 24026704600971
Direct Marking 04026704600977

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10.5 Inch