AccessGUDID - DEVICE: Motion Medical Distributing (15060498450277)

GUDID

Device Identifier (DI) Information

Brand Name: Motion Medical Distributing
Version or Model: 1719
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 1719
Company Name: Haslam Medical, Inc.

Primary DI Number: 15060498450277
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 604208868 *Terms of Use

Device Description: #1719 Obstetrical Kit Contents: (1) Umbilical Scissor, (2) Umbilical Clamp, (1) Bulb Syringe, (1) Underpad 17x24, (1) Receiving Blanket, (2) Towel 3-Ply, (2) Sponge 4x4 2/Pk, (1) OB Pad, (2) Glove L/F Pair, (2) OB Towelette, (1) Apron, (1) Infant Diaper, (1) Bunting Bunting, (2) Twist Tie, (1) Placenta Bag

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":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	Yes
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?
60644	Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use	A collection of various sterile surgical instruments, dressings/drapes, and materials intended to be used during obstetrical/gynaecological surgery. The kit may be referred to as a procedure pack and is typically comprised of devices that individually are not dedicated to a specific type of obstetrical/gynaecological surgical procedure, but are often supplied together to perform a specific type of obstetrical/gynaecological procedure; it does not contain pharmaceuticals. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OKV	Obstetrical Kit

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: b5e1757d-351c-44b0-ad6f-e621ac76cc30
Public Version Date: October 22, 2018
Public Version Number: 3
DI Record Publish Date: January 31, 2017