FDA UDI In Commercial Distribution 🇺🇸 United States

saypha MagIQ

DI: 00362032907017 · Model: 39507 · Obagi Cosmeceuticals LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
saypha MagIQ
Primary DI
00362032907017
Version / Model
39507
Company Name
Obagi Cosmeceuticals LLC
Labeler DUNS
790553353
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-27
Public Version
1
Public Version Date
2025-12-05
Public Version Status
New
Public Device Record Key
eabfcaad-2aba-438d-b602-940f543f437d

Device Description

Dermal HA filler indicated for injection into the mid to deep dermis for correction of moderate to severe facial wrinkles and folds (such as nasolabial folds) in adults over the age of 21.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LMH Implant, Dermal, For Aesthetic Use

GMDN Terms

Code Name
47887 Dermal tissue reconstructive material, microbe-derived, anaesthetic

Identifiers

Type ID
Primary 00362032907017

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 25 Degrees Celsius