FDA UDI In Commercial Distribution 🇺🇸 United States

HIRSCHMAN RECTAL SPECULUM

DI: 00192896087873 · Model: 508-362 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HIRSCHMAN RECTAL SPECULUM
Primary DI
00192896087873
Version / Model
508-362
Catalog Number
508-362
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
1
Public Version Date
2018-10-22
Public Version Status
New
Public Device Record Key
75a740b2-11c1-4f1e-85e2-46a3b60c57cf

Device Description

HIRSCHMAN RECTAL SPECULUM MEDIUM SIZE

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
FFQ SPECULUM, RECTAL

GMDN Terms

Code Name
35351 Rectal speculum

Identifiers

Type ID
Primary 00192896087873

Customer Contacts

Device Sizes

Type Value Unit Text
Length 2.625 Inch
Lumen/Inner Diameter 0.6875 Inch