FDA UDI In Commercial Distribution 🇺🇸 United States

Guedel Airway

DI: 00709078006838 · Model: 7-3571 · WESTMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Guedel Airway
Primary DI
00709078006838
Version / Model
7-3571
Company Name
WESTMED, INC.
Labeler DUNS
092673953
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2019-05-06
Public Version
1
Public Version Date
2019-05-14
Public Version Status
New
Public Device Record Key
a79a0d28-3cdf-4002-9fc4-fbd7b002e49c

Device Description

Guedel Airway 70 mm White

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
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAE Airway, Oropharyngeal, Anesthesiology

GMDN Terms

Code Name
42420 Oesophageal-obturating/tracheal airway, single-use

Identifiers

Type ID
Primary 00709078006838
Unit of Use 10709078006828