AccessGUDID - DEVICE: Warming Cabinet (00850038811242)

GUDID

Device Identifier (DI) Information

Brand Name: Warming Cabinet
Version or Model: 7922TPTGG
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 14B7922279
Company Name: Blickman Industries, LLC

Primary DI Number: 00850038811242
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 076681238 *Terms of Use

Device Description: Warming Cabinet Pass Through 30"W x 35 1/2"H x 26 1/2"D w/(2) Glass Doors w/(2) Adj Shelves

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
45334	Multi-purpose warming cabinet, recessed	A mains electricity (AC-powered) built-in device designed to warm various items and products prior to use, e.g., bags of irrigation or intravenous (IV) solutions, blankets or clothing to cover or put onto a patient, or clothing for the operating room (OR) personnel to adorn. It typically consists of a heat insulated enclosure with a sealing door, shelves, heating element(s), a thermostat and operating controls. This is a cabinet that is built into the room construction (recessed into the wall) so that it does not take any floor space of, e.g., the OR. It may also be used in a laboratory.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LHC	Warmer, Irrigation Solution

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 4bb61894-687a-4d79-bb51-c869c1748981
Public Version Date: April 19, 2022
Public Version Number: 1
DI Record Publish Date: April 11, 2022