FDA UDI In Commercial Distribution 🇺🇸 United States

INGE LAMINA SPREADER

DI: 00192896038004 · Model: 417-064C · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
INGE LAMINA SPREADER
Primary DI
00192896038004
Version / Model
417-064C
Catalog Number
417-064C
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
4
Public Version Date
2026-03-05
Public Version Status
Update
Public Device Record Key
30ecce07-9339-4955-aa3a-d4b704e68a5f

Device Description

INGE LAMINA SPREADER PEDIATRIC TIP C

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
FFO RETRACTOR, SELF-RETAINING

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896038004

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.5 Inch