FDA UDI In Commercial Distribution 🇺🇸 United States

Plastipak

DI: 07501073025530 · Model: 302553 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Plastipak
Primary DI
07501073025530
Version / Model
302553
Catalog Number
302553
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
001292192
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-17
Public Version
1
Public Version Date
2024-06-25
Public Version Status
New
Public Device Record Key
aacca300-2b89-4851-aebe-ec8a376c585d

Device Description

SYRINGE 5ML LL SYRINGE ONLY MX BUN

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
FMF Syringe, piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Package 17501073025537
Primary 07501073025530
Package 50382903025539

Premarket Submissions

Submission Number Supplement Number
K151766 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature