FDA UDI In Commercial Distribution 🇺🇸 United States

M-Flex®

DI: 00816734020227 · Model: 1206-10 · DIVERSATEK HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
M-Flex®
Primary DI
00816734020227
Version / Model
1206-10
Catalog Number
1206-10
Company Name
DIVERSATEK HEALTHCARE, INC.
Labeler DUNS
030650113
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
7
Public Version Date
2019-04-10
Public Version Status
Update
Public Device Record Key
e739429d-8ab4-4159-a335-eb8a96a6fb52

Device Description

Blue Silicone Tungsten Maloney Bougie Mini-Set

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
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
FAT Bougie, Esophageal, And Gastrointestinal, Gastro-Urology

GMDN Terms

Code Name
35052 Oesophageal bougie, reusable

Identifiers

Type ID
Primary 00816734020227

Customer Contacts

Phone
800-558-6408

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store flat, do not hang