FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00812480010079 · Model: 2420CE · MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00812480010079
Version / Model
2420CE
Catalog Number
2420CE
Company Name
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC.
Labeler DUNS
790265227
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2023-06-01
Public Version Status
Update
Public Device Record Key
6befc452-2ec4-439a-8104-a7ff24d26923

Device Description

23 Gauge Vitreous Cutter, 25 psi, Luer Posterior PVC Tubing Set, Sterile, Single Use

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
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

GMDN Terms

Code Name
59258 Vitrectomy system micro-cutting unit

Identifiers

Type ID
Package 10812480010076
Primary 00812480010079

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K102222 000

Device Sizes

Type Value Unit Text
Needle Gauge 23 Gauge

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 98 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
10 – 98 Percent (%) Relative Humidity