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Assi

FDA UDI

Class I (US FDA UDI)

by Accurate Surgical & Scientific Instruments Corp.

Identity

Trade Name
ASSI FDA UDI
Generic Name
Tenotome FDA UDI
Device Name
Tenolysis Double Ended Pulley Dilator 3-5mm and 4-6mm FDA UDI
Model / Reference
ASSI.22009 FDA UDI
Description
Tenolysis Double Ended Pulley Dilator 3-5mm and 4-6mm FDA UDI

Identifiers

Primary DI / UDI-DI
00841645115380 FDA UDI
FDA Product Code
HXB FDA UDI
GMDN Term
Tenotome 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

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

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: Tenotome

Assi by Accurate Surgical & Scientific Instruments Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tenotome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 73bbf473-5c2c-4000-9626-bb8f36e67733 33 fields · synced Jun 1, 2026