AccessGUDID - DEVICE: P&P Medical Surgical LLC (G026022301)

GUDID

Device Identifier (DI) Information

Brand Name: P&P Medical Surgical LLC
Version or Model: 03100
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: P&P Medical Surgical LLC

Primary DI Number: G026022301
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 022925151 *Terms of Use

Device Description: Disposable Safety Scalpels Sterile Surgical Blade Size 11 Stainless Steel with Plastic Handle & Metric Line Individually Foil Wrapped Box of 10

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":	No
For Single-Use:	Yes
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?
47569	Scalpel, single-use	A hand-held, manual surgical instrument constructed as a one-piece handle and scalpel blade (not an exchangeable component) used by the operator to manually cut or dissect tissue. The blade is typically made of high-grade stainless steel alloy or carbon steel and the handle is often made of plastic. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GDX	Scalpel, One-Piece

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: Yes
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: 902b4ba6-a605-45a8-bb81-0cdb5f34c449
Public Version Date: January 12, 2022
Public Version Number: 1
DI Record Publish Date: January 04, 2022