FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: 00709078013560 · Model: WP-7704 · WESTMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
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Primary DI
00709078013560
Version / Model
WP-7704
Company Name
WESTMED, INC.
Labeler DUNS
092673953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-15
Public Version
1
Public Version Date
2021-10-25
Public Version Status
New
Public Device Record Key
31a9e01f-f843-4e58-ab20-cf46ab8d3af2

Device Description

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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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BYE Attachment, Breathing, Positive End Expiratory Pressure

GMDN Terms

Code Name
46823 PEEP valve, single-use

Identifiers

Type ID
Package 10709078013574
Primary 00709078013560