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Knap Stainless Steel Retractor for Laser (non glare)

FDA UDI

Class I (US FDA UDI)

by Oculo-Plastik Inc

Identity

Trade Name
Knap Stainless Steel Retractor for Laser (non glare) FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
The Knap is a retractor, with four curved narrow blunt strips. All non-reflective. FDA UDI
Model / Reference
28-010 FDA UDI
Description
The Knap is a retractor, with four curved narrow blunt strips. All non-reflective. FDA UDI

Identifiers

Primary DI / UDI-DI
10697660003723 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Knap Stainless Steel Retractor for Laser (non glare) by Oculo-Plastik Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oculo-Plastik Inc

Sources (1)

  • FDA UDI be6e0dc6-c1d8-4eb1-b5c5-524e428be596 35 fields · synced May 30, 2026