FDA UDI In Commercial Distribution 🇺🇸 United States

WEITLANER RETRACTOR

DI: 00192896049192 · Model: 1100-642 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WEITLANER RETRACTOR
Primary DI
00192896049192
Version / Model
1100-642
Catalog Number
1100-642
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
3
Public Version Date
2019-08-28
Public Version Status
Update
Public Device Record Key
95d57a58-f725-4e42-97bd-113cf8e92824

Device Description

WEITLANER RETRACTOR HINGED BLUNT TIPS

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
GAD Retractor

GMDN Terms

Code Name
33542 Bone hook

Identifiers

Type ID
Primary 00192896049192

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.25 Inch