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STILLE Retractors

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
STILLE Retractors FDA UDI
Generic Name
Nerve/vessel retractor FDA UDI
Device Name
NERVE RETRACTOR LOVE STILLE 7 mm 20.5 cm 8 in FDA UDI
Model / Reference
108-26048-7 FDA UDI
Description
NERVE RETRACTOR LOVE STILLE 7 mm 20.5 cm 8 in FDA UDI

Identifiers

Catalog Number
108-26048-7 FDA UDI
Primary DI / UDI-DI
07332339212209 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Nerve/vessel retractor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 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

Dimensions & Sizes

Size
Length — 20.5 Centimeter FDA UDI

Category: Nerve/vessel retractor

STILLE Retractors by Stille AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nerve/vessel retractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 6b0efda4-66d6-4407-bbbf-687475df35f5 36 fields · synced Jun 8, 2026