FDA UDI In Commercial Distribution 🇺🇸 United States

Intradermal Cannulae

DI: 15056030402545 · Model: AE1711-02/40 · STERIMEDIX LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

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
Intradermal Cannulae
Primary DI
15056030402545
Version / Model
AE1711-02/40
Catalog Number
AE1711
Company Name
STERIMEDIX LIMITED
Labeler DUNS
504799313
Distribution Status
In Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2024-10-07
Public Version
1
Public Version Date
2024-10-15
Public Version Status
New
Public Device Record Key
ad61a3cb-3d57-454c-9fa3-4a6649b3a793

Device Description

SILKANN CANNULA 20g x60mm

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
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
MED Sterilant, Medical Devices

GMDN Terms

Code Name
46676 Tissue injection cannula

Identifiers

Type ID
Unit of Use 25056030402542
Primary 15056030402545