AccessGUDID - DEVICE: NATIONAL HOSPITAL PACKAGING (00817213021148)

GUDID

Device Identifier (DI) Information

Brand Name: NATIONAL HOSPITAL PACKAGING
Version or Model: 25-002
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 25-002
Company Name: Surgi-Pak, Inc.

Primary DI Number: 00817213021148
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 152736971 *Terms of Use

Device Description: SAFETY PINS, #3 LARGE 2IN, 2/PKG, STRL

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):	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?
10904	Surgical instrument clip	A device designed to hold surgical instruments together; typically those with ring handles. This can be for sterilization, storage purposes, and/or to keep surgical instruments used for a particular procedure together prior to being lain out for surgery. It is typically designed like a very large safety pin (i.e., an elongated spring wire clasp with a locking catch onto which the instruments are threaded, usually by the ring handle). It is typically made of stainless steel or chromed metal. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MDM	Instrument, Manual, Surgical, General Use

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: 784cb8d9-f586-4069-9e4d-2a9e2ac24d20
Public Version Date: May 08, 2023
Public Version Number: 2
DI Record Publish Date: December 05, 2022

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
00817213022305	96	00817213021148		In Commercial Distribution	Case

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 6269683335
Email: orders@nhpsurgipak.com

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