FDA UDI In Commercial Distribution 🇺🇸 United States

AUFRICHT RETRACTOR

DI: 00192896025660 · Model: 207-292 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AUFRICHT RETRACTOR
Primary DI
00192896025660
Version / Model
207-292
Catalog Number
207-292
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
2019-11-19
Public Version Status
Update
Public Device Record Key
db897f69-fd29-4478-829f-837c5ba91672

Device Description

AUFRICHT RETRACTOR SOLID 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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
KAL Retractor, Ent

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary 00192896025660

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.5 Inch
Device Size Text, specify 45 Millimeter Tip