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Nabatoff Vein Stripper Set

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
NABATOFF VEIN STRIPPER SET FDA UDI
Generic Name
Vein stripper, reusable FDA UDI
Device Name
NABATOFF VEIN STRIPPER SET WITH STERILIZING CASE STAINLESS STEEL FDA UDI
Model / Reference
170-330 FDA UDI
Description
NABATOFF VEIN STRIPPER SET WITH STERILIZING CASE STAINLESS STEEL FDA UDI

Identifiers

Catalog Number
170-330 FDA UDI
Primary DI / UDI-DI
00192896024342 FDA UDI
FDA Product Code
GAI FDA UDI
GMDN Term
Vein stripper, 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

Category: Vein stripper, reusable

Nabatoff Vein Stripper Set by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vein stripper, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d5e8dd4-241e-4663-9277-5a7510cafaf2 35 fields · synced Jun 8, 2026