FDA UDI In Commercial Distribution 🇺🇸 United States

WEBSTER NEEDLE HOLDER

DI: 00192896081383 · Model: 1100-392 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WEBSTER NEEDLE HOLDER
Primary DI
00192896081383
Version / Model
1100-392
Catalog Number
1100-392
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
2023-10-03
Public Version Status
Update
Public Device Record Key
97fee090-07d9-419f-a8d9-67484b9c656d

Device Description

WEBSTER NEEDLE HOLDER SERRATED BLADE

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
FHQ Holder, Needle, Gastroenterologic

GMDN Terms

Code Name
12726 Suturing needle holder, reusable

Identifiers

Type ID
Primary 00192896081383

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4.75 Inch