FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10195327668723 · Model: DYNJAP9721B · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10195327668723
Version / Model
DYNJAP9721B
Catalog Number
DYNJAP9721B
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-29
Public Version
2
Public Version Date
2024-12-24
Public Version Status
Update
Public Device Record Key
235a5c82-41c0-40cc-a25c-8d32ff59f370

Device Description

ANESTH CIRCUIT PEDI HMEF-LF

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
CAI Circuit, breathing (w connector, adaptor, y piece)

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 40195327668724
Primary 10195327668723

Customer Contacts