FDA UDI In Commercial Distribution 🇺🇸 United States

Skytron

DI: 10841736116262 · Model: F221 SERIES Freedom · SKYTRON LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Skytron
Primary DI
10841736116262
Version / Model
F221 SERIES Freedom
Catalog Number
F221 SERIES
Company Name
SKYTRON LLC
Labeler DUNS
078375583
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-20
Public Version
1
Public Version Date
2021-10-28
Public Version Status
New
Public Device Record Key
4b11aa6e-b4c2-4b4e-abc3-029838b1de15

Device Description

F221 SERIES MD/LD TWIN TANDEM

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FQO TABLE, OPERATING-ROOM, AC-POWERED

GMDN Terms

Code Name
35630 General utility supply system, ceiling-mounted

Identifiers

Type ID
Primary 10841736116262

Customer Contacts