FDA UDI In Commercial Distribution 🇺🇸 United States

CASPAR LUMBAR SPECULA

DI: 00192896079441 · Model: 416-827 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASPAR LUMBAR SPECULA
Primary DI
00192896079441
Version / Model
416-827
Catalog Number
416-827
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
4
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
2a3a429e-7805-429f-852e-b4e1e04dd8e3

Device Description

CASPAR LUMBAR SPECULUM NON-REFLECTIVE BLACK ANNODIZED COATED

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
FXE Speculum, Non-Illuminated

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896079441

Customer Contacts

Device Sizes

Type Value Unit Text
Width 18 Millimeter
Length 85 Millimeter