FDA UDI In Commercial Distribution 🇺🇸 United States

DUALX DUAL PORTAL SERIAL DILATOR #7

DI: B707MDSD20020 · Model: MDSD2002 · Amplify Surgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DUALX DUAL PORTAL SERIAL DILATOR #7
Primary DI
B707MDSD20020
Version / Model
MDSD2002
Company Name
Amplify Surgical, Inc.
Labeler DUNS
081021000
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-18
Public Version
1
Public Version Date
2022-11-28
Public Version Status
New
Public Device Record Key
209ed75e-7239-4fd7-bbcc-0610c9f59fbd

Device Description

SERIAL DILATOR #7

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
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary B707MDSD20020

Customer Contacts

Phone
7652675439

Premarket Submissions

Submission Number Supplement Number
K181397 000