FDA UDI In Commercial Distribution 🇺🇸 United States

HARTMANN-HALLE NASAL SPECULUM

DI: 00192896018358 · Model: 16-2322 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HARTMANN-HALLE NASAL SPECULUM
Primary DI
00192896018358
Version / Model
16-2322
Catalog Number
16-2322
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-17
Public Version
2
Public Version Date
2019-10-28
Public Version Status
Update
Public Device Record Key
f0edd5d8-b2fd-478b-b718-1729fd498e99

Device Description

HARTMANN-HALLE NASAL SPECULUM MEDIUM BLADES

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
EPY SPECULUM, ENT

GMDN Terms

Code Name
35350 Nasal speculum, reusable

Identifiers

Type ID
Primary 00192896018358

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6 Inch