← Back to catalogue

Sentient Manufacturing

FDA UDI

Class II (US FDA UDI)

by Sentient Manufacturing , LLC

Identity

Trade Name
Sentient Manufacturing FDA UDI
Generic Name
Laser fibre stripper FDA UDI
Device Name
Sentient Manufacturing Laser Fiber Stripper Blades FDA UDI
Model / Reference
3041350 FDA UDI
Description
Sentient Manufacturing Laser Fiber Stripper Blades FDA UDI

Identifiers

Primary DI / UDI-DI
00860007603761 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Laser fibre stripper FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laser fibre stripper

Sentient Manufacturing by Sentient Manufacturing , LLC — Class II — 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

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

Manufacturer

Manufacturer
Sentient Manufacturing , LLC

Sources (1)

  • FDA UDI 24ab1112-910f-4996-9dc3-257128f56abb 33 fields · synced May 31, 2026