FDA UDI In Commercial Distribution 🇺🇸 United States

CASPAR LUMBAR SPECULA

DI: 00192896096363 · Model: 416-823 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASPAR LUMBAR SPECULA
Primary DI
00192896096363
Version / Model
416-823
Catalog Number
416-823
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-09
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
9b2ed8ee-3e9c-456e-bb03-e11d3c704f58

Device Description

CASPAR LUMBAR SPECULUM BLACK ANODIZED 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
Yes
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
FXE Speculum, Non-Illuminated

GMDN Terms

Code Name
35048 Bone lever/elevator, reusable

Identifiers

Type ID
Primary 00192896096363

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Device Size Text, specify 55 x 18 Millimeters