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Endotrig

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
ENDOTRIG FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Device Name
System FDA UDI
Model / Reference
1010 FDA UDI
Description
System FDA UDI

Identifiers

Catalog Number
1010 FDA UDI
Primary DI / UDI-DI
07613327356113 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Manual scalpel blade, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual scalpel blade, single-use

Endotrig by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual scalpel blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI d2a5128e-0e65-43d0-bd77-5f41460a327d 34 fields · synced May 30, 2026