GII Ethibond

GII SNAP-PAK SNAP-PAK Size 2 (5 metric) green ETHIBOND braided polyester suture, 36 Inches (91cm), double-armed with CP-2 needles

Registry build 21.09.26
1manufacturer
2catalogue numbers in this listing

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code GAS
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for GII Ethibond
Listed by DePuy Mitek, Inc., United States
FDA product code GAS
Device type Suture, Nonabsorbable, Synthetic, Polyester
Device class Class 2
Regulation 21 CFR 878.5000
Establishment Specification developer, Manufacturer
Premarket notification Exempt
Record published 2015-09-01
Record revised 2021-09-27 (version 6)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature up to 77 °F; Storage environment temperature up to 25 °C; Handling environment temperature up to 77 °F; Handling environment temperature up to 25 °C
Packaging Package of 5
Distribution end date 2021-01-28

Catalogue Numbers

Catalogue numbers for GII Ethibond
Catalogue number Size Status
216593 Withdrawn
216193 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Atramat Internacional Farmacéutica S.A DE C.V 49
TopLock Fusion Orthopedics, LLC 33
RAM® COR-Suture® Quick Load® LSI Solutions Inc. 15
A.C.S® (Alcon Closure System) Alcon Laboratories, Inc. 10
Riverbond Riverpoint Medical LLC 7
Polybond Riverpoint Medical LLC 6
Fast-FIX Smith & Nephew, Inc. 3
COR-Suture® Quick Load® LSI Solutions Inc. 2
RD® Quick Load® LSI Solutions Inc. 2
Rapidloc Ethibond DePuy Mitek, Inc. 2
ALLthread Titanium Biomet Orthopedics 2
Bioknotless Panacryl Ethibond DePuy Mitek, Inc. 1

Showing 12 of 16. All products under Suture, Nonabsorbable, Synthetic, Polyester

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P880094 1989-09-22 DACRON SURGICAL SUTURES Alcon Laboratories, Inc.
P840041 1989-08-08 NOVAFIL(TM) Davis & Geck, Inc.
N83509 1987-02-20 NON-ABSORBABLE (POLYESTER FIBER) SUTURES Davis & Geck, Inc.
N17809 1986-12-03 ETHIBOND* Ethicon, Inc.
N80950 1985-03-22 POLYVIOLENE SUTURE Look, Inc.
N17804 1984-03-27 ETHIBOND* Ethicon, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer