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Stripper Scribe Tool

FDA UDI

Class I (US FDA UDI)

by Optical Integrity, Inc.

Identity

Trade Name
Stripper Scribe Tool FDA UDI
Generic Name
Laser fibre stripper FDA UDI
Model / Reference
11382 FDA UDI

Identifiers

Primary DI / UDI-DI
00810077631447 FDA UDI
FDA Product Code
HRT FDA UDI
GMDN Term
Laser fibre stripper FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 25 Millimeter FDA UDI

Category: Laser fibre stripper

Stripper Scribe Tool by Optical Integrity, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laser fibre stripper.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 00a702a0-dbbc-4317-890d-2132e3955dfe 35 fields · synced May 30, 2026