FDA UDI In Commercial Distribution 🇺🇸 United States

LATEX O-RINGS

DI: 00192896044685 · Model: 508-551 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LATEX O-RINGS
Primary DI
00192896044685
Version / Model
508-551
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-07
Public Version
1
Public Version Date
2018-10-08
Public Version Status
New
Public Device Record Key
0d9c450e-f741-47fb-9fae-bb44fdc8e5fa

Device Description

LATEX O-RINGS REGULAR (100 PER BAG)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
FHN Ligator, Hemorrhoidal

GMDN Terms

Code Name
35157 Haemorrhoid ligator

Identifiers

Type ID
Previous B0995085510
Primary 00192896044685

Customer Contacts

Phone
800-821-7496