FDA UDI In Commercial Distribution 🇺🇸 United States

Primrose Medical, Inc

DI: 00852323007293 · Model: 900-5130 · Primrose Medical Inc
Product Codes
1
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Primrose Medical, Inc
Primary DI
00852323007293
Version / Model
900-5130
Company Name
Primrose Medical Inc
Labeler DUNS
617604392
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-25
Public Version
2
Public Version Date
2023-03-20
Public Version Status
Update
Public Device Record Key
f19986f9-6008-4644-88a7-0f256852ef5c

Device Description

Sub-Q ( subcutaneous ) Administration set, Safety

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
17180 Subcutaneous infusion/injection port needle
36244 Electronic gravity infusion controller administration set
46846 Mechanical infusion pump administration set
35833 Electric infusion pump administration set, single-use

Identifiers

Type ID
Primary 00852323007293

Premarket Submissions

Submission Number Supplement Number
K920537 000