FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094009798 · Model: 901117 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094009798
Version / Model
901117
Catalog Number
328044-506
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-01
Public Version
2
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
fda5c601-5c75-4a1d-a74b-2fba31df3f01

Device Description

OBTURATOR ASSM F 33220 & 33320

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
No
Sterilization Prior Use
No

Product Codes

Code Name
FER Anoscope and accessories

GMDN Terms

Code Name
10156 Optical anoscope, reusable

Identifiers

Type ID
Primary 00732094009798

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K810227 000