← Back to catalogue

Kaye Blepharoplasty Scissors

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Kaye Blepharoplasty Scissors FDA UDI
Generic Name
Blepharoplasty scissors FDA UDI
Device Name
Kaye Blepharoplasty Scissors Straight Serrated Blade Power Cut Silver Ribbon Handle FDA UDI
Model / Reference
13-6800 FDA UDI
Description
Kaye Blepharoplasty Scissors Straight Serrated Blade Power Cut Silver Ribbon Handle FDA UDI

Identifiers

Primary DI / UDI-DI
00192896114654 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Blepharoplasty scissors FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 4.25 Inch FDA UDI

Category: Blepharoplasty scissors

Kaye Blepharoplasty Scissors by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blepharoplasty scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI fb0be152-4dbe-468c-be5c-d4b613a12069 35 fields · synced May 30, 2026