FDA UDI In Commercial Distribution 🇺🇸 United States

KELLY DECEMET MEMBRANE PUNCH

DI: 00192896012769 · Model: 11-9270 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KELLY DECEMET MEMBRANE PUNCH
Primary DI
00192896012769
Version / Model
11-9270
Catalog Number
11-9270
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-12
Public Version
1
Public Version Date
2018-10-15
Public Version Status
New
Public Device Record Key
1382b4cc-9692-4456-a59b-f3b11df2518a

Device Description

KELLY DESCEMETS MEMBRANE PUNCH DEEP BITE

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
HNJ Punch, corneo-scleral

GMDN Terms

Code Name
13232 Corneoscleral punch

Identifiers

Type ID
Primary 00192896012769

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 1 Millimeter
Device Size Text, specify 0.75 Millimeter Bite