Identity
- Trade Name
- Berghaus/Schrom FDA UDI
- Generic Name
- Eyelid weight, implantable FDA UDI
- Device Name
- Lid-Chain Berghaus/Schrom 0.6GM FDA UDI
- Model / Reference
- 28-1506 FDA UDI
- Description
- Lid-Chain Berghaus/Schrom 0.6GM FDA UDI
Identifiers
- Catalog Number
- 28-1506 FDA UDI
- Primary DI / UDI-DI
- M6332815060 FDA UDI
- 510(k) Number
- K021750 FDA UDI
- FDA Product Code
- MML FDA UDI
- GMDN Term
- Eyelid weight, implantable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5700 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Weight — 0.6 Gram FDA UDI
Category: Eyelid weight, implantable
Berghaus/Schrom by JEDMED Instrument Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K021750 also covers:
- Berghaus/Schrom — JEDMED Instrument Company
- Berghaus/Schrom — JEDMED Instrument Company
- Berghaus/Schrom — JEDMED Instrument Company
- Berghaus/Schrom — JEDMED Instrument Company
- Berghaus/Schrom — JEDMED Instrument Company
- Berghaus/Schrom — JEDMED Instrument Company
- Berghaus/Schrom — JEDMED Instrument Company
- Lid implant (lid chain) — Spiggle & Theis Medizintechnik GmbH
- Lid implant (lid chain) — Spiggle & Theis Medizintechnik GmbH
- Lid implant (lid chain) — Spiggle & Theis Medizintechnik GmbH
- Lid implant (lid chain) — Spiggle & Theis Medizintechnik GmbH
- Lid implant (lid chain) — Spiggle & Theis Medizintechnik GmbH
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- JEDMED Instrument Company
Sources (1)
- FDA UDI adc0ad52-281e-44b9-acd4-187ea4a90b9b 37 fields · synced May 30, 2026