AccessGUDID - DEVICE: eShield Cell Phone Size (M266EC21000)

GUDID

Device Identifier (DI) Information

Brand Name: eShield Cell Phone Size
Version or Model: EC2100
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Whitney Medical Solutions

Primary DI Number: M266EC21000
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 119676187 *Terms of Use

Device Description: The Whitney Medical Solutions’ eShield consists of polyethylene film (and an adhesive pad in some models) with tear guide that allows the cover to be torn fairly straight across it. There is also a double sided tape that is used as a closure method with the cover being folded twice and sealed against it. The device is provided to the user sterile, is labeled for single use only and not intended for resterilization or reprocessing. The sterile eShield is sterilized using a validated irradiation sterilization method.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
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:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
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?
12535	Medical equipment/instrument drape, single-use	A flexible polymer sheet/bag/sleeve designed to form a protective water-resistant enclosure around a piece of medical equipment/instrument (e.g., C-arm, surgical laser/camera/microscope, examination table/chair) and/or components (e.g., cables, tubes, headrest). It is intended as a hygienic barrier to protect the equipment/instrument from soiling and/or contamination when used inside, or within the vicinity of, a hygienic area; it may have patient contact, however it is not intended to be introduced into a body cavity (noninvasive). It is neither a dedicated handle cover, device cap nor an ultrasound transducer cover. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KKX	Drape, Surgical

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K141438	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Radiation Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Width: 36 Centimeter
Depth: 22 Centimeter
Width: 23 Centimeter
Depth: 11 Centimeter

Device Record Status

Public Device Record Key: 7dd55f7f-7f44-4c2a-8d2b-ea03b06bceff
Public Version Date: September 11, 2024
Public Version Number: 9
DI Record Publish Date: September 20, 2016