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Stratte Scissors

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
STRATTE SCISSORS FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, reusable FDA UDI
Device Name
STRATTE SCISSORS HEAVY S-CURVED FDA UDI
Model / Reference
508-606 FDA UDI
Description
STRATTE SCISSORS HEAVY S-CURVED FDA UDI

Identifiers

Catalog Number
508-606 FDA UDI
Primary DI / UDI-DI
00192896044845 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Flexible endoscopic biopsy forceps, reusable 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

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 — 10 Inch FDA UDI

Category: Flexible endoscopic biopsy forceps, reusable

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

Similar devices

Also classified as Flexible endoscopic biopsy forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 88fc94ad-74d7-4c69-9bcc-e7f2c644041e 36 fields · synced May 30, 2026