FDA UDI In Commercial Distribution 🇺🇸 United States

SafeGuide®

DI: 00816734020975 · Model: 1214-02 · DIVERSATEK HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SafeGuide®
Primary DI
00816734020975
Version / Model
1214-02
Catalog Number
1214-02
Company Name
DIVERSATEK HEALTHCARE, INC.
Labeler DUNS
030650113
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-17
Public Version
6
Public Version Date
2019-04-10
Public Version Status
Update
Public Device Record Key
c00e76db-f5b4-429d-ae1f-d5ceb56add9b

Device Description

Guidewire with Spring Tip

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "High-level Disinfectant"]

Product Codes

Code Name
KNQ Dilator, Esophageal

GMDN Terms

Code Name
35009 Over-guidewire oesophageal dilator

Identifiers

Type ID
Package 10816734020972
Primary 00816734020975

Customer Contacts

Phone
800-558-6408

Device Sizes

Type Value Unit Text
Length 210 Centimeter