FDA UDI In Commercial Distribution 🇺🇸 United States

SafeGuide® Single

DI: 00816734023334 · Model: 1215-60 · DIVERSATEK HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SafeGuide® Single
Primary DI
00816734023334
Version / Model
1215-60
Catalog Number
1215-60
Company Name
DIVERSATEK HEALTHCARE, INC.
Labeler DUNS
030650113
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-14
Public Version
1
Public Version Date
2023-08-22
Public Version Status
New
Public Device Record Key
14fcb1cd-36c5-4b14-af2b-939a1fa7eed0

Device Description

Disposable Over the Guidewire Esophageal Dilator, 60 FR

Device Characteristics

Single Use
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KNQ Dilator, Esophageal

GMDN Terms

Code Name
35009 Over-guidewire oesophageal dilator

Identifiers

Type ID
Primary 00816734023334

Customer Contacts

Phone
800-558-6408