FDA UDI In Commercial Distribution 🇺🇸 United States

Centurion

DI: 10653160263661 · Model: I67875K · CENTURION MEDICAL PRODUCTS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Centurion
Primary DI
10653160263661
Version / Model
I67875K
Catalog Number
I67875K
Company Name
CENTURION MEDICAL PRODUCTS CORPORATION
Labeler DUNS
017246562
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-01
Public Version
1
Public Version Date
2022-01-10
Public Version Status
New
Public Device Record Key
a606df44-ce91-4933-8d29-2a02536f350c

Device Description

ST REPROCESSED WEBSTER NHLDR (OR2200K)

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
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
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
62479 Surgical soft-tissue manipulation forceps, tweezers-like, single-use

Identifiers

Type ID
Package 00653160263664
Primary 10653160263661

Customer Contacts