AccessGUDID - DEVICE: SCANLAN® (00846159004076)

GUDID

Device Identifier (DI) Information

Brand Name: SCANLAN®
Version or Model: 3786-28
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 3786-28
Company Name: SCANLAN INTERNATIONAL INC

Primary DI Number: 00846159004076
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 023055619 *Terms of Use

Device Description: Yasargil Applying Forceps

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:	No
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?
34951	Bulldog clamp	A manual surgical instrument with heavily serrated jaws at the working end designed to grasp, join, compress or support an organ, vessel or tissue. This instrument is typically made of high-grade stainless steel and comes in two main designs: 1) a flat, pincer-like design with jaws that close to a set opening and which have serrated finger grips or opposing handles at the proximal end which, when depressed by the operator, release the clamp; or 2) a self-retaining, scissors-like design with ring handles; both may have various straight, angled or curved blades at the working end. This is a reusable device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
GDJ	Clamp, Surgical, General & Plastic Surgery

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: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

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: d38c21ce-9470-4559-b0ca-cade8013141e
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: January 06, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

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: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 651-298-0997
Email: VanderpoelW@Scanlangroup.com

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