FDA UDI In Commercial Distribution 🇺🇸 United States

PILLING

DI: 24026704516982 · Model: IPN005333 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PILLING
Primary DI
24026704516982
Version / Model
IPN005333
Catalog Number
343505
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
2021-01-18
Public Version Status
Update
Public Device Record Key
aa4041c6-8be1-4267-8d8e-c78ab4f86d88

Device Description

BRUNS CURETTE SIZE 3 9"

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
No
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
KBJ CURETTE, ADENOID

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 24026704516982
Direct Marking 04026704516988

Customer Contacts

Device Sizes

Type Value Unit Text
Length 9 Inch