← Back to catalogue

Assi

FDA UDI

Class I (US FDA UDI)

by Accurate Surgical & Scientific Instruments Corp.

Identity

Trade Name
ASSI FDA UDI
Generic Name
Surgical instrument/implant rack FDA UDI
Device Name
Satellight Needle Holder Forceps, 15cm Lg., Rnd. Hdl. 8mm Dia., Ctr. Bal., Cvd. 45' Angle To The Side, Tip 0.6mm Dia. FDA UDI
Model / Reference
ASSI.NHFA15RM8 FDA UDI
Description
Satellight Needle Holder Forceps, 15cm Lg., Rnd. Hdl. 8mm Dia., Ctr. Bal., Cvd. 45' Angle To The Side, Tip 0.6mm Dia. FDA UDI

Identifiers

Primary DI / UDI-DI
00841645112686 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Surgical instrument/implant rack 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

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: Surgical instrument/implant rack

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

Similar devices

Also classified as Surgical instrument/implant rack.

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

Sources (1)

  • FDA UDI 6aa512ff-d298-4a21-a20d-6477cd39a65f 33 fields · synced May 31, 2026