Deknatel

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: DEKNATEL FDA UDI
Generic Name: Operative-site suture holder FDA UDI
Device Name: GABBAY-FRATER SUTORGANIZER (4 PIECES OF 1) FDA UDI
Model / Reference: IPN912380 FDA UDI
Description: GABBAY-FRATER SUTORGANIZER (4 PIECES OF 1) FDA UDI

Identifiers

Catalog Number: GFS-1A FDA UDI
Primary DI / UDI-DI: 14026704626707 FDA UDI
FDA Product Code: FZX FDA UDI
GMDN Term: Operative-site suture holder FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Depth — 0.75 Inch FDA UDI
Length — 9 Inch FDA UDI
Width — 1.5 Inch FDA UDI

Category: Operative-site suture holder

Deknatel by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI 6fb422ea-6c77-466d-87f7-1db8d175316e 36 fields · synced May 30, 2026