FDA UDI In Commercial Distribution 🇺🇸 United States

Procedure Products Syringe

DI: B1604930Y211 · Model: 4930-Y21 · PROCEDURE PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Procedure Products Syringe
Primary DI
B1604930Y211
Version / Model
4930-Y21
Company Name
PROCEDURE PRODUCTS, INC.
Labeler DUNS
151507563
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-07
Public Version
4
Public Version Date
2018-09-12
Public Version Status
Update
Public Device Record Key
1e73b0df-e65a-438d-a7e0-6f4f045341b2

Device Description

10CC L.L. YELLOW SYRINGE W/ CONTRAST LABEL

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
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
Primary B1604930Y211

Premarket Submissions

Submission Number Supplement Number
K874747 000