AccessGUDID - DEVICE: STILLE Wire Twisting and Holding Forceps (07332339211660)

GUDID

Device Identifier (DI) Information

Brand Name: STILLE Wire Twisting and Holding Forceps
Version or Model: 104-15854
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 104-15854
Company Name: Stille AB

Primary DI Number: 07332339211660
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 355280827 *Terms of Use

Device Description: WIRE HOLDING FORCEPS STILLE double-joint fine 18 cm 7 in

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):	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?
32886	Wire holding/twisting forceps	A surgical instrument with specially designed sturdy blades used to grip, tighten and/or twist wires that are being applied to the patient during a surgical intervention. It typically has a scissors-like design with ring handles, is made of high-grade stainless steel and may be self-retaining. It is available in various sizes and the working end can have a variety of jaw designs, e.g., typically short and broad with carbide inserts, but some may be long with side protruding posts around which the loose end of the wire are secured to provide greater grip. The blades/handles are typically strong in profile. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HXP	Instrument, Bending Or Contouring

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
Length: 18 Centimeter

Device Record Status

Public Device Record Key: 8ed07c26-683b-4450-bdbe-4d741f50cd71
Public Version Date: October 02, 2020
Public Version Number: 1
DI Record Publish Date: September 24, 2020