FDA UDI In Commercial Distribution 🇺🇸 United States

Ultra RapidWarm Blast

DI: 17350025914258 · Model: 10150 · Vitrolife Sweden AB
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

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Basic Information

Brand Name
Ultra RapidWarm Blast
Primary DI
17350025914258
Version / Model
10150
Company Name
Vitrolife Sweden AB
Labeler DUNS
631805488
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2024-09-16
Public Version
1
Public Version Date
2024-09-24
Public Version Status
New
Public Device Record Key
160e41fb-dc5f-4910-838e-9ffbd066e93c

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQL Media, Reproductive

GMDN Terms

Code Name
44046 IVF medium

Identifiers

Type ID
Unit of Use 07350025914251
Primary 17350025914258

Premarket Submissions

Submission Number Supplement Number
K240605 000