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#10- Blunt Hook, 90°, Length 191mm, .8mm Tip

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
#10- Blunt Hook, 90°, Length 191mm, .8mm Tip FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
#10- Blunt Hook, 90°, Length 191mm, .8mm Tip FDA UDI
Model / Reference
N7110-K FDA UDI
Description
#10- Blunt Hook, 90°, Length 191mm, .8mm Tip FDA UDI

Identifiers

Primary DI / UDI-DI
00840096204674 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Hand-held surgical retractor, reusable 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Hand-held surgical retractor, reusable

#10- Blunt Hook, 90°, Length 191mm, .8mm Tip by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d7045a03-5a22-43e5-958a-3099d5586677 33 fields · synced May 30, 2026