FDA UDI In Commercial Distribution 🇺🇸 United States

BODENHAMMER RECTAL SPECULUM

DI: 00192896044296 · Model: 508-315 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BODENHAMMER RECTAL SPECULUM
Primary DI
00192896044296
Version / Model
508-315
Catalog Number
508-315
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
1
Public Version Date
2018-10-15
Public Version Status
New
Public Device Record Key
3b3bcef2-5a9e-4d39-a44c-a61222153921

Device Description

BODENHAMMER RECTAL SPECULUM WITH SCREW SET

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
FFQ SPECULUM, RECTAL

GMDN Terms

Code Name
35351 Rectal speculum

Identifiers

Type ID
Primary 00192896044296

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6 Inch