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Alexandra Muscle Hook

FDA UDI

Class I (US FDA UDI)

by Blink Medical Limited

Identity

Trade Name
Alexandra Muscle Hook FDA UDI
Generic Name
Soft-tissue surgical hook, single-use FDA UDI
Model / Reference
90-5005 FDA UDI

Identifiers

Primary DI / UDI-DI
05060480408142 FDA UDI
FDA Product Code
HNQ FDA UDI
GMDN Term
Soft-tissue surgical hook, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Soft-tissue surgical hook, single-use

Alexandra Muscle Hook by Blink Medical Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue surgical hook, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9dcd9988-a658-4934-9ac7-85eb11780871 32 fields · synced Jun 8, 2026