FDA UDI In Commercial Distribution 🇺🇸 United States

Ritter

DI: 00841709106743 · Model: 255-002 · MIDMARK CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ritter
Primary DI
00841709106743
Version / Model
255-002
Catalog Number
255-002
Company Name
MIDMARK CORPORATION
Labeler DUNS
005036025
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-31
Public Version
5
Public Version Date
2021-02-23
Public Version Status
Update
Public Device Record Key
59b0509a-0239-406d-a7b4-dbdc9194a602

Device Description

The Ritter 9' Single Ceiling Mount LED Procedure Light is intended to be used in medical environments where illumination is required for medical use during external examinations and procedures.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KZF Device, medical examination, ac powered

GMDN Terms

Code Name
12276 Fixed examination/treatment room light

Identifiers

Type ID
Primary 00841709106743

Customer Contacts

Storage Conditions

Type
Handling Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Storage Environment Temperature
Temperature Range
-30 – 60 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Handling Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-30 – 60 Degrees Celsius