AccessGUDID - DEVICE: Spectrum, Inc. (00855495007351)

GUDID

Device Identifier (DI) Information

Brand Name: Spectrum, Inc.
Version or Model: 982-03954-001
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: SD-100
Company Name: SPECTRUM, INC.

Primary DI Number: 00855495007351
Issuing Agency: GS1
Commercial Distribution End Date: July 03, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 080458964 *Terms of Use

Device Description: Sterile Equipment Drape, 12" X 100" w/Bag Clip, Latex Free

Device Characteristics

What MRI safety information does the labeling contain?	MR Safe
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":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
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?
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
LPZ	Container, frozen donor tissue storage

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K934630	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
Ethylene Oxide

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: 2101c9fe-7716-4d9c-9b98-51980589b7e5
Public Version Date: September 11, 2024
Public Version Number: 7
DI Record Publish Date: July 21, 2017