FDA UDI In Commercial Distribution 🇺🇸 United States

HARTMAN PUNCH

DI: 00192896080300 · Model: 478-312 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HARTMAN PUNCH
Primary DI
00192896080300
Version / Model
478-312
Catalog Number
478-312
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-20
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
d4190908-e574-43c9-953e-6d2ae687e7b5

Device Description

HARTMAN PUNCH ROUND JAW #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
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
KBS PUNCH, ADENOID

GMDN Terms

Code Name
36199 ENT soft-tissue cutting forceps

Identifiers

Type ID
Primary 00192896080300

Customer Contacts

Device Sizes

Type Value Unit Text
Length 5.5 Inch
Device Size Text, specify 7 Millimeter Jaw