FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094215748 · Model: 901057 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094215748
Version / Model
901057
Catalog Number
4200B
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-05
Public Version
8
Public Version Date
2020-09-22
Public Version Status
Update
Public Device Record Key
de77a0bb-deb8-46c4-a83e-7a6e4d244e20

Device Description

SPOT PLANNING PARENT-BP ONLY

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQA Oximeter

GMDN Terms

Code Name
57960 Multiple physiological parameter spot-check system, clinical

Identifiers

Type ID
Primary 00732094215748
Package 00732094006599

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K101680 000