FDA UDI In Commercial Distribution 🇺🇸 United States

Haritex Corporation

DI: 04719880180530 · Model: HC-33 · HARITEX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1000

Basic Information

Brand Name
Haritex Corporation
Primary DI
04719880180530
Version / Model
HC-33
Catalog Number
HC-33
Company Name
HARITEX CORPORATION
Labeler DUNS
656398765
Distribution Status
In Commercial Distribution
Device Count in Pkg
1000
Record Status
Published
Publish Date
2023-08-21
Public Version
1
Public Version Date
2023-08-29
Public Version Status
New
Public Device Record Key
761bc824-3ea3-4d70-b207-0080caead77b

Device Description

Thumb forceps, 5", single use. Zi

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEN Forceps, General & Plastic Surgery

GMDN Terms

Code Name
62489 Dressing/utility forceps, tweezers-like, single-use

Identifiers

Type ID
Package 14719880180544
Primary 04719880180530
Unit of Use 04719880180363