FDA UDI In Commercial Distribution 🇺🇸 United States

PILLING

DI: 14026704805232 · Model: IPN021089 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PILLING
Primary DI
14026704805232
Version / Model
IPN021089
Catalog Number
P26444
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
3095a6b3-ce41-4361-ad03-cfb4b4fb7ef1

Device Description

BAYONET NEEDLE FINE 6 1/2"

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
Yes
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
KBR NEEDLE, TONSIL SUTURING

GMDN Terms

Code Name
46549 Eye spud/needle

Identifiers

Type ID
Direct Marking 54026704805230
Primary 14026704805232

Customer Contacts