FDA UDI Not in Commercial Distribution 🇺🇸 United States

FOLLISTIM AQ Cartridge 600IU

DI: 00300520316019 · Model: 1022678 · Merck Sharp & Dohme LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FOLLISTIM AQ Cartridge 600IU
Primary DI
00300520316019
Version / Model
1022678
Company Name
Merck Sharp & Dohme LLC
Labeler DUNS
101740835
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-14
Public Version
4
Public Version Date
2024-01-01
Public Version Status
Update
Public Device Record Key
7ed2c73a-7d9f-40e9-bcd7-9c95f1917ba7
Distribution End Date
2023-12-31

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
Yes
PM Exempt
No
Has Serial Number
Yes
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
FMI Needle, hypodermic, single lumen

GMDN Terms

Code Name
44127 Autoinjector needle

Identifiers

Type ID
Package 60300520316011
Primary 00300520316019

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 29 Gauge