FDA UDI In Commercial Distribution 🇺🇸 United States

SONTEC GELPI RETRACTOR

DI: 00192896026544 · Model: 230-360 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SONTEC GELPI RETRACTOR
Primary DI
00192896026544
Version / Model
230-360
Catalog Number
230-360
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-11
Public Version
2
Public Version Date
2022-11-01
Public Version Status
Update
Public Device Record Key
c8ae4ef2-51e8-40c8-ba1d-cac98ca5fa52

Device Description

SONTEC GELPI RETRACTOR MULTIPLE LEVEL PARALLEL SHARP TIP

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
GAD Retractor

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00192896026544

Customer Contacts

Device Sizes

Type Value Unit Text
Length 12 Inch
Device Size Text, specify 10 Millimeter Tip